FDA Import Refusal AEK-1705849-3/1/1 — Aurobindo Pharma USA Inc
The FDA refused shipment AEK-1705849-3/1/1 from Aurobindo Pharma USA Inc (United States) on Jan 26, 2016. The refused product falls under Drugs and Biologics — VENLAFAXINE HYDROCHLORIDE (ANTI-DEPRESSANT). Cited charge: 75 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Jan 26, 2016
- Country
- United States
- Product Category
- Drugs and Biologics
- Product Code
- 61NDY80 VENLAFAXINE HYDROCHLORIDE (ANTI-DEPRESSANT)
- Charges
- 75