FDA Import Refusal AEK-0492552-4/50002/1 — Glenmark Pharmaceuticals Limited

Glenmark Pharmaceuticals Limited — FEI 3005757050

The FDA refused shipment AEK-0492552-4/50002/1 from Glenmark Pharmaceuticals Limited (India) on May 27, 2026. 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 27, 2026
Country
India
Product Category
Drugs and Biologics
Product Code
62OCA09 TELMISARTAN (ANTI-HYPERTENSIVE - PART II)
Charges
27