FDA Import Refusal AEK-0832619-0/10002/1 — Acme Lifetech LLP

Acme Lifetech LLP — FEI 3013998702

The FDA refused shipment AEK-0832619-0/10002/1 from Acme Lifetech LLP (India) on Jul 16, 2026. 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
Jul 16, 2026
Country
India
Product Category
Drugs and Biologics
Product Code
62OCA09 TELMISARTAN (ANTI-HYPERTENSIVE - PART II)
Charges
75

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