BRYREL SYRUP

FDA Premarket Approval N17796

Pre-market Approval Supplement Details

• Device: BRYREL SYRUP
• Applicant: SANOFI AVENTIS U.S. LLC
• Date Received: 1975-09-19
• Decision Date: 1976-06-28
• PMA: N17796
• Supplement: S
• Advisory Committee: Ophthalmic
• Expedited Review: No
• Combination Product: No
• Applicant Address: SANOFI AVENTIS U.S. LLC 55 Corporate Drive bridgewater, NJ 08807

Supplemental Filings

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Supplement Number	Date	Supplement Type
N17796		Original Filing