FDA Import Refusal AEK-0679067-8/30002/1 — Glenmark Pharmaceuticals Limited

Glenmark Pharmaceuticals Limited — FEI 3005757050

The FDA refused shipment AEK-0679067-8/30002/1 from Glenmark Pharmaceuticals Limited (India) on Jun 22, 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
Jun 22, 2026
Country
India
Product Category
Drugs and Biologics
Product Code
62OCB09 TELMISARTAN (ANTI-HYPERTENSIVE - PART II)
Charges
27

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.