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Drugs
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Information for Industry (Drugs)
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Advisory Committees Electronic Regulatory Submission and Review Guidances (Drugs) Drug Applications for Over-the-Counter Drugs Paragraph IV Patent Certifications Postmarket Drug Safety Information for Patients and Providers Prescription Drug User Fee Act (PDUFA) Warning Letters and Notice of Violation Letters to Pharmaceutical Companies
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Contact Us
Human Drug Information
- (888) 463-6332
- (301) 796-3400
- druginfo@fda.hhs.gov
Division of Drug Information (CDER)
Office of Communications
WO51-2201
10903 New Hampshire Avenue
Silver Spring, MD 20993
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