Aurobindo Pharma USA Inc recalls Venlafaxine Hydrochloride extended release capsules, 37.5 mg, 30-count bottles, Rx Only, Manufactured for: Aurobindo Pha
Recalled February 22, 2017 · FDA recall D-0474-2017 · Aurobindo Pharma USA
Hazard
Failed Tablet/Capsule Specifications: Some bottles contain punctured, and/or clumped/melted capsules. · FDA Class II
Units
47,040 bottles
Sold at
Nationwide in the US
Description
Failed Tablet/Capsule Specifications: Some bottles contain punctured, and/or clumped/melted capsules.
Product
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
Manufacturer(s)
Aurobindo Pharma USA Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →