FDA Import Refusal AEK-6404423-1/21/1 — EUROFARMA
The FDA refused shipment AEK-6404423-1/21/1 from EUROFARMA (Brazil) on Sep 20, 2024. The refused product falls under Drugs and Biologics — TOPIRAMATE (ANTI-CONVULSANT). Cited charge: 75 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Sep 20, 2024
- Country
- Brazil
- Product Category
- Drugs and Biologics
- Product Code
- 61MCY40 TOPIRAMATE (ANTI-CONVULSANT)
- Charges
- 75