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Mylan Laboratories Limited, (Nashik FDF) recalls Amlodipine and Valsartan Tablets, USP 5/320 mg, 30-count bottles, Rx Only, Made in India, Manufactured for: Mylan Pharma

Recalled December 19, 2018 · FDA recall D-0322-2019 · Mylan Laboratories Limited, (Nashik FDF)

Hazard
GCMP Deviations: FDA analysis confirmed presence of trace amounts of an impurity, N-nitrosodiethylamine (NDEA) found in the API used to manufacture the product. · FDA Class II
Units
109,314 HDPE bottles
Sold at
Product was distributed throughout the United States to several major distributors, including Puerto Rico.

Description

GCMP Deviations: FDA analysis confirmed presence of trace amounts of an impurity, N-nitrosodiethylamine (NDEA) found in the API used to manufacture the product.

Product
Amlodipine and Valsartan Tablets, USP 5/320 mg, 30-count bottles, Rx Only, Made in India, Manufactured for: Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 U.S.A., NDC 0378-1723-93.
Manufacturer(s)
Mylan Laboratories Limited, (Nashik FDF)
Made in
India

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Mylan Laboratories Limited, (Nashik FDF) recalls Amlodipine and Valsartan Tablets, USP 5/320 mg, 30-count bottles, Rx Only, Made in India, Manufactured for: Mylan Pharma | RecallWatchUSA