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Application to Market a New Drug, Biologic or an Antibiotic Drug for Human Use
General Licensing Provisions: Biologics License Application, Changes to an Approved Application, Labeling; and Revocation and Suspension
Form #:   356 h
Agency:  Department of Health and Human Services
Bureau:  Food and Drug Administration
Common Name:   Analysis and Evaluation, Drugs
  TYPE PAGES SIZE (KB) CAPABILITY WHAT'S
NEEDED
pdf Form Only 4 265 [3] Fillable + Printable Adobe Reader Download  

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