Class II
Terminated
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
This recall has been terminated (originally issued February 22, 2017).
- Company
- Aurobindo Pharma Usa Inc
- Recall Initiated
- December 22, 2016
- Posted
- February 22, 2017
- Recall Number
- D-0474-2017
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 47,040 bottles
- Firm Location
- Plainsboro, NJ, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Failed Tablet/Capsule Specifications: Some bottles contain punctured, and/or clumped/melted capsules.
Distribution
Nationwide in the US
Lot / Code Info
Lot #: VI3716010-A, Exp. 04/2018
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