FDA Import Refusal AEK-4845091-8/41/1 — Rottendorf Pharma Gmbh
The FDA refused shipment AEK-4845091-8/41/1 from Rottendorf Pharma Gmbh (Germany) on Mar 18, 2024. 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
- Mar 18, 2024
- Country
- Germany
- Product Category
- Drugs and Biologics
- Product Code
- 62ODY09 TELMISARTAN (ANTI-HYPERTENSIVE - PART II)
- Charges
- 118,75