FDAFDA · Food and drugs·Recall number D-0474-2017
Venlafaxine Hydrochloride extended release capsules, 37.5 mg, 30-count bottles, Rx Only, Manufactured for: Aurobindo Pharma USA, Inc. 2400 Route 130 North, Dayton, NJ 08810 Manufactured by: Aurobindo Pharma Limited Hyderabad-500 072 India, NDC 65862-527-30
Published February 22, 2017 · Recall initiated: December 22, 2016
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Tablet/Capsule Specifications: Some bottles contain punctured, and/or clumped/melted capsules.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- VENLAFAXINE HYDROCHLORIDE
- Manufacturer
- Aurobindo Pharma USA Inc
- Distributor
- Nationwide in the US
- UPC
- 0365862528476
- Lot
- Lot #: VI3716010-A, Exp. 04/2018
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.