FDA Import Refusal AEK-2027330-5/20003/1 — GLENMARK PHARMACEUTICALS LTD

GLENMARK PHARMACEUTICALS LTD — FEI 3019089903

The FDA refused shipment AEK-2027330-5/20003/1 from GLENMARK PHARMACEUTICALS LTD (India) on Oct 21, 2026. The refused product falls under Drugs and Biologics — TELMISARTAN (ANTI-HYPERTENSIVE - PART II). Cited charge: 75 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Oct 21, 2026
Country
India
Product Category
Drugs and Biologics
Product Code
62OCA09 TELMISARTAN (ANTI-HYPERTENSIVE - PART II)
Charges
75

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