FDA Import Refusal AEK-8260094-9/41/1 — Sanofi Aventis
The FDA refused shipment AEK-8260094-9/41/1 from Sanofi Aventis (Tunisia) on March 19, 2025. The refused product falls under Drugs and Biologics — QUININE DIHYDROCHLORIDE (ANTI-PROTOZOAL, A-LEISHMANIAL, A-MALARIAL). Cited charge: 75 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- March 19, 2025
- Country
- Tunisia
- Product Category
- Drugs and Biologics
- Product Code
- 62LDY36 QUININE DIHYDROCHLORIDE (ANTI-PROTOZOAL, A-LEISHMANIAL, A-MALARIAL)
- Charges
- 75