FDA Import Refusal AEK-4893039-8/31/1 — GLENMARK PHARMACEUTICALS LTD
The FDA refused shipment AEK-4893039-8/31/1 from GLENMARK PHARMACEUTICALS LTD (India) on Mar 21, 2024. The refused product falls under Drugs and Biologics — MINOXIDIL (ANTI-HYPERTENSIVE). Cited charge: 75 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Mar 21, 2024
- Country
- India
- Product Category
- Drugs and Biologics
- Product Code
- 62CDL41 MINOXIDIL (ANTI-HYPERTENSIVE)
- Charges
- 75