FDA Import Refusal AEK-2214280-5/60003/1 — GLENMARK PHARMACEUTICALS LTD

GLENMARK PHARMACEUTICALS LTD — FEI 3019089903

The FDA refused shipment AEK-2214280-5/60003/1 from GLENMARK PHARMACEUTICALS LTD (India) on Oct 6, 2026. The refused product falls under Drugs and Biologics — TELMISARTAN (ANTI-HYPERTENSIVE - PART II). Cited charges: 118,75 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Oct 6, 2026
Country
India
Product Category
Drugs and Biologics
Product Code
62ODA09 TELMISARTAN (ANTI-HYPERTENSIVE - PART II)
Charges
118,75

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