Home / Import refusals / AEK-7840360-5/90003/1

FDA Import Refusal AEK-7840360-5/90003/1 — GLENMARK PHARMACEUTICAL

GLENMARK PHARMACEUTICAL — FEI 3017590933

The FDA refused shipment AEK-7840360-5/90003/1 from GLENMARK PHARMACEUTICAL (India) on Nov 13, 2025. The refused product falls under Drugs and Biologics — TELMISARTAN (ANTI-HYPERTENSIVE - PART II). Cited charge: 75 This firm has 3 other import refusals on record.

Refusal Details

Date
Nov 13, 2025
Country
India
Product Category
Drugs and Biologics
Product Code
62OCA09 TELMISARTAN (ANTI-HYPERTENSIVE - PART II)
Charges
75

Other import refusals

FDA data resources

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