Zydus Pharmaceuticals USA Inc recalls Venlafaxine HCL ER Capsule USP, 75mg, packaged in a) 30-count bottles (NDC 68382-035-06), b) 90-count bottles (NDC 68382
Recalled August 24, 2016 · FDA recall D-1461-2016 · Zydus Pharmaceuticals USA
Hazard
Failed Dissolution Specifications: out of specification dissolution results in retained samples · FDA Class II
Units
N/A
Sold at
Nationwide
Description
Failed Dissolution Specifications: out of specification dissolution results in retained samples
Product
Venlafaxine HCL ER Capsule USP, 75mg, packaged in a) 30-count bottles (NDC 68382-035-06), b) 90-count bottles (NDC 68382-035-16), and c) 1000-count bottles, (NDC 68382-035-10), Rx only, Manufactured by : Cadila Healthcare Ltd. Ahmedabad, India, Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08534.
Manufacturer(s)
Zydus Pharmaceuticals USA Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →