FDA Import Refusal AEK-7455478-1/20002/1 — Eurofarma Laboratorios S.A.
The FDA refused shipment AEK-7455478-1/20002/1 from Eurofarma Laboratorios S.A. (Brazil) on Sep 12, 2025. The refused product falls under Drugs and Biologics — ALENDRONATE SODIUM (BONE CALCIUM REGULATOR). Cited charge: 75 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Sep 12, 2025
- Country
- Brazil
- Product Category
- Drugs and Biologics
- Product Code
- 63ADY02 ALENDRONATE SODIUM (BONE CALCIUM REGULATOR)
- Charges
- 75