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Form 356h Application to Market a New Drug or Biologic for Human U
ICR 201701-0910-012 · OMB 0910-0338 · Object 70861801.
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Next Page Export Data Import Data Reset Form Form Approved: OMB No. 0910-0338 Expiration Date: January 31, 2017 See PRA Statement on page 3. DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration APPLICATION TO MARKET A NEW OR ABBREVIATED NEW DRUG OR BIOLOGIC FOR HUMAN USE 1. Date of Submission (mm/dd/yyyy) (Title 21, Code of Federal Regulations, Parts 314 & 601) 2. Name of Applicant APPLICANT INFORMATION 3. Telephone Number (Include country code if applicable and area code) 4. Facsimile (FAX) Number (Include country code if applicable and area code) 5. Applicant Address Address 1 (Street address, P.O. box, company name c/o) Email Address Address 2 (Apartment, suite, unit, building, floor, etc.) City State/Province/Region Country U.S. License Number if previously issued ZIP or Postal Code 6. Authorized U.S. Agent (Required for non-U.S. applicants) Authorized U.S. Agent Name Telephone Number (Include area code) Address 1 (Street address, P.O. box, company name c/o) FAX Number (Include area code) Address 2 (Apartment, suite, unit, building, floor, etc.) City State Email Address ZIP Code 7. NDA, ANDA, or BLA Application Number PRODUCT DESCRIPTION 8. Supplement Number (If applicable) 9. Established Name (e.g., proper name, USP/USAN name) 10. Proprietary Name (Trade Name) (If any) 11. Chemical/Biochemical/Blood Product Name (If any) 12. Dosage Form 13. Strengths 15. Proposed Indication for Use 14. Route of Administration Is this indication for a rare disease (prevalence <200,000 in U.S.)? Does this product have an FDA Orphan Designation for this indication? Yes No 16. Application Type (Select one) APPLICATION INFORMATION 17. If an NDA, identify the type 505 (b)(1) If yes, provide the Orphan Designation number for this indication: New Drug Application (NDA) Yes No Contin. Page for #15 Biologics License Application (BLA) Abbreviated New Drug Application (ANDA) 18. If a BLA, identify the type 505 (b)(2) 351 (a) 351 (k) 19. If a 351(k), identify the biological reference product that is the basis for the submission. Name of Biologic: Holder of Licensed Application: 20. If an ANDA, or 505(b)(2), identify the listed drug product that is the basis for the submission. Name of Drug: Application Number of Relied Upon Product: Indicate Patent Certification(s): P1 21. Submission (Select one) Original Product Correspondence P2 P3 P4 Labeling Supplement REMS Supplement Section viii - MOU CMC Supplement Statement of no relevant patents Efficacy Supplement Postmarketing Requirements or Commitments Annual Report Periodic Safety Report Other (Specify): FORM FDA 356h (1/14) Page 1 of 3 PSC Publishing Services (301) 443-6740 EF Previous Page 22. Submission Sub-Type Next Page Presubmission Amendment Initial Submission Resubmission 24. Does this submission contain only pediatric data? 23. If a supplement, identify the appropriate category. Yes CBE Prior Approval (PA) CBE-30 No 25. Reasons for Submission 26. Proposed Marketing Status (Select one) 27. This application is (Select one) Prescription Product (Rx) Paper Paper and Electronic Over-The-Counter Product (OTC) Electronic 28. Number of Volumes Submitted 29. Establishment Information (Full establishment information should be provided in the body of the application.) Refer to the instruction sheet (Form FDA 356h Supplement) for more information. Establishment Name Address 1 (Street address, P.O. box, company name c/o) Registration (FEI) Number Address 2 (Apartment, suite, unit, building, floor, etc.) MF Number State/Province/Region City Country ZIP or Postal Code Is the establishment new to the application? Yes Establishment DUNS Number What is the status of the establishment? Pending Active No Inactive Withdrawn Establishment Contact Information Name of Contact for the Establishment Telephone Number (Include area code) Address 1 (Street address, P.O. box, company name c/o) FAX Number (Include area code) Address 2 (Apartment, suite, unit, building, floor, etc.) City State/Province/Region Country Email Address ZIP or Postal Code Is the site ready Yes for inspection? If No, when will site be ready? (mm/dd/yyyy) Manufacturing Steps and/or Type of Testing No N/A Continuation Page for #29 30. Cross References (List related BLAs, INDs, NDAs, PMAs, 510(k)s, IDEs, BMFs, MAFs, and DMFs referenced in the current application.) Contin. Page for #30 31. This application contains the following items (Select all that apply) 1. Index 2. Labeling (Select one): 4. Chemistry Section Draft Labeling Final Printed Labeling 3. Summary (21 CFR 314.50 (c)) A. Chemistry, manufacturing, and controls information (e.g., 21 CFR 314.50(d)(1); 21 CFR 601.2) B. Samples (21 CFR 314.50 (e)(1); 21 CFR 601.2 (a)) (Submit only upon FDA’s request) C. Methods validation package (e.g., 21 CFR 314.50(e)(2)(i); 21 CFR 601.2) 5. Nonclinical pharmacology and toxicology section (e.g., 21 CFR 314.50(d)(2); 21 CFR 601.2) 6. Human pharmacokinetics and bioavailability section (e.g., 21 CFR 314.50(d)(3); 21 CFR 601.2) 7. Clinical microbiology section (e.g., 21 CFR 314.50(d)(4)) 8. Clinical data section (e.g., 21 CFR 314.50(d)(5); 21 CFR 601.2) Item 31 continued on page 3 FORM FDA 356h (1/14) Page 2 of 3 Previous Page Next Page 31. This application contains the following items (Continued; select all that apply) 9. Safety update report (e.g., 21 CFR 314.50(d)(5)(vi)(b); 21 CFR 601.2) 10. Statistical section (e.g., 21 CFR 314.50(d)(6); 21 CFR 601.2) 11. Case report tabulations (e.g., 21 CFR 314.50(f)(1); 21 CFR 601.2) 12. Case report forms (e.g., 21 CFR 314.50 (f)(2); 21 CFR 601.2) 13. Patent information on any patent that claims the drug/ biologic (21 U.S.C. 355(b) or (c)) 14. A patent certification with respect to any patent that claims the drug/biologic (21 U.S.C. 355 (b)(2) or (j)(2)(A)) 15. Establishment description (21 CFR Part 600, if applicable) 16. Debarment certification (FD&C Act 306 (k)(1)) 17. Field copy certification (21 CFR 314.50 (l)(3)) 18. User Fee Cover Sheet (PDUFA Form FDA 3397, GDUFA Form FDA 3794, BsUFA Form FDA 3792, or MDUFMA Form FDA 3601) 19. Financial Disclosure Information (21 CFR Part 54) 20. Other (Specify): CERTIFICATION I agree to update this application with new safety information about the product that may reasonably affect the statement of contraindications, warnings, precautions, or adverse reactions in the draft labeling. I agree to submit safety update reports as provided for by regulation or as requested by FDA. If this application is approved, I agree to comply with all applicable laws and regulations that apply to approved applications, including, but not limited to, the following: 1. Good manufacturing practice regulations in 21 CFR Parts 210, 211 or applicable regulations, Parts 606, and/or 820. 2. Biological establishment standards in 21 CFR Part 600. 3. Labeling regulations in 21 CFR Parts 201, 606, 610, 660, and/or 809. 4. In the case of a prescription drug or biological product, prescription drug advertising regulations in 21 CFR Part 202. 5. Regulations on making changes in application in FD&C Act section 506A, 21 CFR 314.71, 314.72, 314.97, 314.99, and 601.12. 6. Regulations on Reports in 21 CFR 314.80, 314.81, 600.80, and 600.81. 7. Local, state, and Federal environmental impact laws. If this application applies to a drug product that FDA has proposed for scheduling under the Controlled Substances Act, I agree not to market the product until the Drug Enforcement Administration makes a final scheduling decision. The data and information in this submission have been reviewed and, to the best of my knowledge, are certified to be true and accurate. Warning: A willfully false statement is a criminal offense, U.S. Code, title 18, section 1001. 32. Typed Name and Title of Applicant’s Responsible Official 34. Telephone Number (Include country code if applicable and area code) 33. Date (mm/dd/yyyy) 35. FAX Number (Include country code if applicable and area code) 36. Email Address 37. Address of Applicant’s Responsible Official Address 1 (Street address, P.O. box, company name c/o) Address 2 (Apartment, suite, unit, building, floor, etc.) City State/Province/Region Country ZIP or Postal Code 38. Signature of Applicant’s Responsible Official or Other Authorized Official Sign 39. Countersignature of Authorized U.S. Agent Sign The information below applies only to requirements of the Paperwork Reduction Act of 1995. The burden time for this collection of information is estimated to average 24 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden to the address to the right: Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff@fda.hhs.gov “An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number.” DO NOT SEND YOUR COMPLETED FORM TO THIS PRA STAFF EMAIL ADDRESS. FORM FDA 356h (1/14) Page 3 of 3 Remove Continuation Page Return to Form FIRST CONTINUATION PAGE FOR ITEM 15 – Proposed Indication for Use Please fill out as many sets of answers as needed, completing all elements within each set that you start. Proposed Indication for Use Is this indication for a rare disease (prevalence <200,000 in U.S.)? Does this product have an FDA Orphan Designation for this indication? Yes No Proposed Indication for Use Proposed Indication for Use Proposed Indication for Use Proposed Indication for Use Proposed Indication for Use Proposed Indication for Use Proposed Indication for Use Proposed Indication for Use Remove Continuation Page FORM FDA 356h (1/14) Yes No Yes No Yes No Yes No Yes No If yes, provide the Orphan Designation number for this indication: Is this indication for a rare disease (prevalence <200,000 in U.S.)? Does this product have an FDA Orphan Designation for this indication? Yes No No If yes, provide the Orphan Designation number for this indication: Is this indication for a rare disease (prevalence <200,000 in U.S.)? Does this product have an FDA Orphan Designation for this indication? Yes No Yes If yes, provide the Orphan Designation number for this indication: Is this indication for a rare disease (prevalence <200,000 in U.S.)? Does this product have an FDA Orphan Designation for this indication? Yes No No If yes, provide the Orphan Designation number for this indication: Is this indication for a rare disease (prevalence <200,000 in U.S.)? Does this product have an FDA Orphan Designation for this indication? Yes No Yes If yes, provide the Orphan Designation number for this indication: Is this indication for a rare disease (prevalence <200,000 in U.S.)? Does this product have an FDA Orphan Designation for this indication? Yes No No If yes, provide the Orphan Designation number for this indication: Is this indication for a rare disease (prevalence <200,000 in U.S.)? Does this product have an FDA Orphan Designation for this indication? Yes No Yes If yes, provide the Orphan Designation number for this indication: Is this indication for a rare disease (prevalence <200,000 in U.S.)? Does this product have an FDA Orphan Designation for this indication? Yes No No If yes, provide the Orphan Designation number for this indication: Is this indication for a rare disease (prevalence <200,000 in U.S.)? Does this product have an FDA Orphan Designation for this indication? Yes No Yes If yes, provide the Orphan Designation number for this indication: Add Second Continuation Page for #15 Return to Form Page X of X Remove Continuation Page Return to Form SECOND CONTINUATION PAGE FOR ITEM 15 – Proposed Indication for Use Please fill out as many sets of answers as needed, completing all elements within each set that you start. Proposed Indication for Use Is this indication for a rare disease (prevalence <200,000 in U.S.)? Does this product have an FDA Orphan Designation for this indication? Yes No Proposed Indication for Use Proposed Indication for Use Proposed Indication for Use Proposed Indication for Use Proposed Indication for Use Proposed Indication for Use Proposed Indication for Use Proposed Indication for Use Remove Continuation Page FORM FDA 356h (1/14) Return to Form Page X of X Yes No Yes No Yes No Yes No Yes No If yes, provide the Orphan Designation number for this indication: Is this indication for a rare disease (prevalence <200,000 in U.S.)? Does this product have an FDA Orphan Designation for this indication? Yes No No If yes, provide the Orphan Designation number for this indication: Is this indication for a rare disease (prevalence <200,000 in U.S.)? Does this product have an FDA Orphan Designation for this indication? Yes No Yes If yes, provide the Orphan Designation number for this indication: Is this indication for a rare disease (prevalence <200,000 in U.S.)? Does this product have an FDA Orphan Designation for this indication? Yes No No If yes, provide the Orphan Designation number for this indication: Is this indication for a rare disease (prevalence <200,000 in U.S.)? Does this product have an FDA Orphan Designation for this indication? Yes No Yes If yes, provide the Orphan Designation number for this indication: Is this indication for a rare disease (prevalence <200,000 in U.S.)? Does this product have an FDA Orphan Designation for this indication? Yes No No If yes, provide the Orphan Designation number for this indication: Is this indication for a rare disease (prevalence <200,000 in U.S.)? Does this product have an FDA Orphan Designation for this indication? Yes No Yes If yes, provide the Orphan Designation number for this indication: Is this indication for a rare disease (prevalence <200,000 in U.S.)? Does this product have an FDA Orphan Designation for this indication? Yes No No If yes, provide the Orphan Designation number for this indication: Is this indication for a rare disease (prevalence <200,000 in U.S.)? Does this product have an FDA Orphan Designation for this indication? Yes No Yes If yes, provide the Orphan Designation number for this indication: Remove Continuation Page Return to Form FIRST CONTINUATION PAGE FOR ITEM 29 – Establishment Information Provide information for additional establishments below, as needed. Establishment Name Address 1 (Street address, P.O. box, company name c/o) Registration (FEI) Number Address 2 (Apartment, suite, unit, building, floor, etc.) City MF Number State/Province/Region Country ZIP or Postal Code Is the establishment new to the application? Yes Establishment DUNS Number What is the status of the establishment? Pending Active No Inactive Withdrawn Establishment Contact Information Name of Contact for the Establishment Telephone Number (Include area code) Address 1 (Street address, P.O. box, company name c/o) FAX Number (Include area code) Address 2 (Apartment, suite, unit, building, floor, etc.) City State/Province/Region Country Email Address ZIP or Postal Code Is the site ready Yes for inspection? If No, when will site be ready? (mm/dd/yyyy) Manufacturing Steps and/or Type of Testing No N/A Establishment Name Address 1 (Street address, P.O. box, company name c/o) Registration (FEI) Number Address 2 (Apartment, suite, unit, building, floor, etc.) City MF Number State/Province/Region Country ZIP or Postal Code Is the establishment new to the application? Yes Establishment DUNS Number What is the status of the establishment? Pending Active No Inactive Withdrawn Establishment Contact Information Name of Contact for the Establishment Telephone Number (Include area code) Address 1 (Street address, P.O. box, company name c/o) FAX Number (Include area code) Address 2 (Apartment, suite, unit, building, floor, etc.) City Country State/Province/Region Email Address ZIP or Postal Code Is the site ready Yes for inspection? If No, when will site be ready? (mm/dd/yyyy) Manufacturing Steps and/or Type of Testing No N/A Add Second Continuation Page for #29 FORM FDA 356h (1/14) Page X of X Remove Continuation Page Return to Form Remove Continuation Page Return to Form SECOND CONTINUATION PAGE FOR ITEM 29 – Establishment Information Provide information for additional establishments below, as needed. Establishment Name Address 1 (Street address, P.O. box, company name c/o) Registration (FEI) Number Address 2 (Apartment, suite, unit, building, floor, etc.) City MF Number State/Province/Region Country ZIP or Postal Code Is the establishment new to the application? Yes Establishment DUNS Number What is the status of the establishment? Pending Active No Inactive Withdrawn Establishment Contact Information Name of Contact for the Establishment Telephone Number (Include area code) Address 1 (Street address, P.O. box, company name c/o) FAX Number (Include area code) Address 2 (Apartment, suite, unit, building, floor, etc.) City State/Province/Region Country Email Address ZIP or Postal Code Is the site ready Yes for inspection? If No, when will site be ready? (mm/dd/yyyy) Manufacturing Steps and/or Type of Testing No N/A Establishment Name Address 1 (Street address, P.O. box, company name c/o) Registration (FEI) Number Address 2 (Apartment, suite, unit, building, floor, etc.) City MF Number State/Province/Region Country ZIP or Postal Code Is the establishment new to the application? Yes Establishment DUNS Number What is the status of the establishment? Pending Active No Inactive Withdrawn Establishment Contact Information Name of Contact for the Establishment Telephone Number (Include area code) Address 1 (Street address, P.O. box, company name c/o) FAX Number (Include area code) Address 2 (Apartment, suite, unit, building, floor, etc.) City Country State/Province/Region Email Address ZIP or Postal Code Is the site ready Yes for inspection? If No, when will site be ready? (mm/dd/yyyy) Manufacturing Steps and/or Type of Testing No N/A Add Third Continuation Page for #29 FORM FDA 356h (1/14) Page X of X Remove Continuation Page Return to Form Remove Continuation Page Return to Form THIRD CONTINUATION PAGE FOR ITEM 29 – Establishment Information Provide information for additional establishments below, as needed. Establishment Name Address 1 (Street address, P.O. box, company name c/o) Registration (FEI) Number Address 2 (Apartment, suite, unit, building, floor, etc.) City MF Number State/Province/Region Country ZIP or Postal Code Is the establishment new to the application? Yes Establishment DUNS Number What is the status of the establishment? Pending Active No Inactive Withdrawn Establishment Contact Information Name of Contact for the Establishment Telephone Number (Include area code) Address 1 (Street address, P.O. box, company name c/o) FAX Number (Include area code) Address 2 (Apartment, suite, unit, building, floor, etc.) City State/Province/Region Country Email Address ZIP or Postal Code Is the site ready Yes for inspection? If No, when will site be ready? (mm/dd/yyyy) Manufacturing Steps and/or Type of Testing No N/A Establishment Name Address 1 (Street address, P.O. box, company name c/o) Registration (FEI) Number Address 2 (Apartment, suite, unit, building, floor, etc.) City MF Number State/Province/Region Country ZIP or Postal Code Is the establishment new to the application? Yes Establishment DUNS Number What is the status of the establishment? Pending Active No Inactive Withdrawn Establishment Contact Information Name of Contact for the Establishment Telephone Number (Include area code) Address 1 (Street address, P.O. box, company name c/o) FAX Number (Include area code) Address 2 (Apartment, suite, unit, building, floor, etc.) City Country State/Province/Region Email Address ZIP or Postal Code Is the site ready Yes for inspection? If No, when will site be ready? (mm/dd/yyyy) Manufacturing Steps and/or Type of Testing No N/A Add Fourth Continuation Page for #29 FORM FDA 356h (1/14) Page X of X Remove Continuation Page Return to Form Remove Continuation Page Return to Form FOURTH CONTINUATION PAGE FOR ITEM 29 – Establishment Information Provide information for additional establishments below, as needed. Establishment Name Address 1 (Street address, P.O. box, company name c/o) Registration (FEI) Number Address 2 (Apartment, suite, unit, building, floor, etc.) City MF Number State/Province/Region Country ZIP or Postal Code Is the establishment new to the application? Yes Establishment DUNS Number What is the status of the establishment? Pending Active No Inactive Withdrawn Establishment Contact Information Name of Contact for the Establishment Telephone Number (Include area code) Address 1 (Street address, P.O. box, company name c/o) FAX Number (Include area code) Address 2 (Apartment, suite, unit, building, floor, etc.) City State/Province/Region Country Email Address ZIP or Postal Code Is the site ready Yes for inspection? If No, when will site be ready? (mm/dd/yyyy) Manufacturing Steps and/or Type of Testing No N/A Establishment Name Address 1 (Street address, P.O. box, company name c/o) Registration (FEI) Number Address 2 (Apartment, suite, unit, building, floor, etc.) City MF Number State/Province/Region Country ZIP or Postal Code Is the establishment new to the application? Yes Establishment DUNS Number What is the status of the establishment? Pending Active No Inactive Withdrawn Establishment Contact Information Name of Contact for the Establishment Telephone Number (Include area code) Address 1 (Street address, P.O. box, company name c/o) FAX Number (Include area code) Address 2 (Apartment, suite, unit, building, floor, etc.) City Country State/Province/Region Email Address ZIP or Postal Code Is the site ready Yes for inspection? If No, when will site be ready? (mm/dd/yyyy) Manufacturing Steps and/or Type of Testing No N/A Add Fifth Continuation Page for #29 FORM FDA 356h (1/14) Page X of X Remove Continuation Page Return to Form Remove Continuation Page Return to Form FIFTH CONTINUATION PAGE FOR ITEM 29 – Establishment Information Provide information for additional establishments below, as needed. Establishment Name Address 1 (Street address, P.O. box, company name c/o) Registration (FEI) Number Address 2 (Apartment, suite, unit, building, floor, etc.) City MF Number State/Province/Region Country ZIP or Postal Code Is the establishment new to the application? Yes Establishment DUNS Number What is the status of the establishment? Pending Active No Inactive Withdrawn Establishment Contact Information Name of Contact for the Establishment Telephone Number (Include area code) Address 1 (Street address, P.O. box, company name c/o) FAX Number (Include area code) Address 2 (Apartment, suite, unit, building, floor, etc.) City State/Province/Region Country Email Address ZIP or Postal Code Is the site ready Yes for inspection? If No, when will site be ready? (mm/dd/yyyy) Manufacturing Steps and/or Type of Testing No N/A Establishment Name Address 1 (Street address, P.O. box, company name c/o) Registration (FEI) Number Address 2 (Apartment, suite, unit, building, floor, etc.) City MF Number State/Province/Region Country ZIP or Postal Code Is the establishment new to the application? Yes Establishment DUNS Number What is the status of the establishment? Pending Active No Inactive Withdrawn Establishment Contact Information Name of Contact for the Establishment Telephone Number (Include area code) Address 1 (Street address, P.O. box, company name c/o) FAX Number (Include area code) Address 2 (Apartment, suite, unit, building, floor, etc.) City Country State/Province/Region Email Address ZIP or Postal Code Is the site ready Yes for inspection? If No, when will site be ready? (mm/dd/yyyy) Manufacturing Steps and/or Type of Testing No N/A Add Sixth Continuation Page for #29 FORM FDA 356h (1/14) Page X of X Remove Continuation Page Return to Form Remove Continuation Page Return to Form SIXTH CONTINUATION PAGE FOR ITEM 29 – Establishment Information Provide information for additional establishments below, as needed. Establishment Name Address 1 (Street address, P.O. box, company name c/o) Registration (FEI) Number Address 2 (Apartment, suite, unit, building, floor, etc.) City MF Number State/Province/Region Country ZIP or Postal Code Is the establishment new to the application? Yes Establishment DUNS Number What is the status of the establishment? Pending Active No Inactive Withdrawn Establishment Contact Information Name of Contact for the Establishment Telephone Number (Include area code) Address 1 (Street address, P.O. box, company name c/o) FAX Number (Include area code) Address 2 (Apartment, suite, unit, building, floor, etc.) City State/Province/Region Country Email Address ZIP or Postal Code Is the site ready Yes for inspection? If No, when will site be ready? (mm/dd/yyyy) Manufacturing Steps and/or Type of Testing No N/A Establishment Name Address 1 (Street address, P.O. box, company name c/o) Registration (FEI) Number Address 2 (Apartment, suite, unit, building, floor, etc.) City MF Number State/Province/Region Country ZIP or Postal Code Is the establishment new to the application? Yes Establishment DUNS Number What is the status of the establishment? Pending Active No Inactive Withdrawn Establishment Contact Information Name of Contact for the Establishment Telephone Number (Include area code) Address 1 (Street address, P.O. box, company name c/o) FAX Number (Include area code) Address 2 (Apartment, suite, unit, building, floor, etc.) City Country State/Province/Region Email Address ZIP or Postal Code Is the site ready Yes for inspection? If No, when will site be ready? (mm/dd/yyyy) Manufacturing Steps and/or Type of Testing No N/A Add Seventh Continuation Page for #29 FORM FDA 356h (1/14) Page X of X Remove Continuation Page Return to Form Remove Continuation Page Return to Form SEVENTH CONTINUATION PAGE FOR ITEM 29 – Establishment Information Provide information for additional establishments below, as needed. Establishment Name Address 1 (Street address, P.O. box, company name c/o) Registration (FEI) Number Address 2 (Apartment, suite, unit, building, floor, etc.) City MF Number State/Province/Region Country ZIP or Postal Code Is the establishment new to the application? Yes Establishment DUNS Number What is the status of the establishment? Pending Active No Inactive Withdrawn Establishment Contact Information Name of Contact for the Establishment Telephone Number (Include area code) Address 1 (Street address, P.O. box, company name c/o) FAX Number (Include area code) Address 2 (Apartment, suite, unit, building, floor, etc.) City State/Province/Region Country Email Address ZIP or Postal Code Is the site ready Yes for inspection? If No, when will site be ready? (mm/dd/yyyy) Manufacturing Steps and/or Type of Testing No N/A Establishment Name Address 1 (Street address, P.O. box, company name c/o) Registration (FEI) Number Address 2 (Apartment, suite, unit, building, floor, etc.) City MF Number State/Province/Region Country ZIP or Postal Code Is the establishment new to the application? Yes Establishment DUNS Number What is the status of the establishment? Pending Active No Inactive Withdrawn Establishment Contact Information Name of Contact for the Establishment Telephone Number (Include area code) Address 1 (Street address, P.O. box, company name c/o) FAX Number (Include area code) Address 2 (Apartment, suite, unit, building, floor, etc.) City Country State/Province/Region Email Address ZIP or Postal Code Is the site ready Yes for inspection? If No, when will site be ready? (mm/dd/yyyy) Manufacturing Steps and/or Type of Testing No N/A Add Eighth Continuation Page for #29 FORM FDA 356h (1/14) Page X of X Remove Continuation Page Return to Form Remove Continuation Page Return to Form EIGHTH CONTINUATION PAGE FOR ITEM 29 – Establishment Information Provide information for additional establishments below, as needed. Establishment Name Address 1 (Street address, P.O. box, company name c/o) Registration (FEI) Number Address 2 (Apartment, suite, unit, building, floor, etc.) City MF Number State/Province/Region Country ZIP or Postal Code Is the establishment new to the application? Yes Establishment DUNS Number What is the status of the establishment? Pending Active No Inactive Withdrawn Establishment Contact Information Name of Contact for the Establishment Telephone Number (Include area code) Address 1 (Street address, P.O. box, company name c/o) FAX Number (Include area code) Address 2 (Apartment, suite, unit, building, floor, etc.) City State/Province/Region Country Email Address ZIP or Postal Code Is the site ready Yes for inspection? If No, when will site be ready? (mm/dd/yyyy) Manufacturing Steps and/or Type of Testing No N/A Establishment Name Address 1 (Street address, P.O. box, company name c/o) Registration (FEI) Number Address 2 (Apartment, suite, unit, building, floor, etc.) City MF Number State/Province/Region Country ZIP or Postal Code Is the establishment new to the application? Yes Establishment DUNS Number What is the status of the establishment? Pending Active No Inactive Withdrawn Establishment Contact Information Name of Contact for the Establishment Telephone Number (Include area code) Address 1 (Street address, P.O. box, company name c/o) FAX Number (Include area code) Address 2 (Apartment, suite, unit, building, floor, etc.) City Country State/Province/Region Email Address ZIP or Postal Code Is the site ready Yes for inspection? If No, when will site be ready? (mm/dd/yyyy) Manufacturing Steps and/or Type of Testing No N/A Add Ninth Continuation Page for #29 FORM FDA 356h (1/14) Page X of X Remove Continuation Page Return to Form Remove Continuation Page Return to Form NINTH CONTINUATION PAGE FOR ITEM 29 – Establishment Information Provide information for additional establishments below, as needed. Establishment Name Address 1 (Street address, P.O. box, company name c/o) Registration (FEI) Number Address 2 (Apartment, suite, unit, building, floor, etc.) City MF Number State/Province/Region Country ZIP or Postal Code Is the establishment new to the application? Yes Establishment DUNS Number What is the status of the establishment? Pending Active No Inactive Withdrawn Establishment Contact Information Name of Contact for the Establishment Telephone Number (Include area code) Address 1 (Street address, P.O. box, company name c/o) FAX Number (Include area code) Address 2 (Apartment, suite, unit, building, floor, etc.) City State/Province/Region Country Email Address ZIP or Postal Code Is the site ready Yes for inspection? If No, when will site be ready? (mm/dd/yyyy) Manufacturing Steps and/or Type of Testing No N/A Establishment Name Address 1 (Street address, P.O. box, company name c/o) Registration (FEI) Number Address 2 (Apartment, suite, unit, building, floor, etc.) City MF Number State/Province/Region Country ZIP or Postal Code Is the establishment new to the application? Yes Establishment DUNS Number What is the status of the establishment? Pending Active No Inactive Withdrawn Establishment Contact Information Name of Contact for the Establishment Telephone Number (Include area code) Address 1 (Street address, P.O. box, company name c/o) FAX Number (Include area code) Address 2 (Apartment, suite, unit, building, floor, etc.) City Country State/Province/Region Email Address ZIP or Postal Code Is the site ready Yes for inspection? If No, when will site be ready? (mm/dd/yyyy) Manufacturing Steps and/or Type of Testing No N/A Add Tenth Continuation Page for #29 FORM FDA 356h (1/14) Page X of X Remove Continuation Page Return to Form Remove Continuation Page Return to Form TENTH CONTINUATION PAGE FOR ITEM 29 – Establishment Information Provide information for additional establishments below, as needed. Establishment Name Address 1 (Street address, P.O. box, company name c/o) Registration (FEI) Number Address 2 (Apartment, suite, unit, building, floor, etc.) City MF Number State/Province/Region Country ZIP or Postal Code Is the establishment new to the application? Yes Establishment DUNS Number What is the status of the establishment? Pending Active No Inactive Withdrawn Establishment Contact Information Name of Contact for the Establishment Telephone Number (Include area code) Address 1 (Street address, P.O. box, company name c/o) FAX Number (Include area code) Address 2 (Apartment, suite, unit, building, floor, etc.) City State/Province/Region Country Email Address ZIP or Postal Code Is the site ready Yes for inspection? If No, when will site be ready? (mm/dd/yyyy) Manufacturing Steps and/or Type of Testing No N/A Establishment Name Address 1 (Street address, P.O. box, company name c/o) Registration (FEI) Number Address 2 (Apartment, suite, unit, building, floor, etc.) City MF Number State/Province/Region Country ZIP or Postal Code Is the establishment new to the application? Yes Establishment DUNS Number What is the status of the establishment? Pending Active No Inactive Withdrawn Establishment Contact Information Name of Contact for the Establishment Telephone Number (Include area code) Address 1 (Street address, P.O. box, company name c/o) FAX Number (Include area code) Address 2 (Apartment, suite, unit, building, floor, etc.) City Country State/Province/Region ZIP or Postal Code Is the site ready Yes for inspection? If No, when will site be ready? (mm/dd/yyyy) Manufacturing Steps and/or Type of Testing FORM FDA 356h (1/14) Email Address Page X of X Remove Continuation Page No N/A Return to Form Remove Continuation Page Return to Form CONTINUATION PAGE FOR ITEM 30 – Cross References Continue your answer in the space below. Remove Continuation Page FORM FDA 356h (1/14) Return to Form Page X of X
| File Type | application/pdf |
| File Title | FDA-356h_clean.indd |
| Author | PSC Publishing Services |
| File Modified | 2014-02-26 |
| File Created | 2014-02-11 |