FDA Import Refusal AEK-8463982-0/31/1 — Glenmark Pharmaceuticals Limited
The FDA refused shipment AEK-8463982-0/31/1 from Glenmark Pharmaceuticals Limited (India) on May 2, 2025. The refused product falls under Drugs and Biologics — TELMISARTAN (ANTI-HYPERTENSIVE - PART II). Cited charge: 27 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- May 2, 2025
- Country
- India
- Product Category
- Drugs and Biologics
- Product Code
- 62ODA09 TELMISARTAN (ANTI-HYPERTENSIVE - PART II)
- Charges
- 27