FDA Import Refusal AEK-2230167-4/60003/1 — Glenmark Pharmaceuticals Limited

Glenmark Pharmaceuticals Limited — FEI 3005757050

The FDA refused shipment AEK-2230167-4/60003/1 from Glenmark Pharmaceuticals Limited (India) on Oct 9, 2026. The refused product falls under Drugs and Biologics — DEXTROMETHORPHAN HYDROBROMIDE (ANTI-TUSSIVE/COLD). Cited charge: 27 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Oct 9, 2026
Country
India
Product Category
Drugs and Biologics
Product Code
62UDL11 DEXTROMETHORPHAN HYDROBROMIDE (ANTI-TUSSIVE/COLD)
Charges
27

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