FDAFebruary 28, 2019drug

BuPROPion Hydrochloride Extended-Release Tablets, USP (XL) 150 mg, a) 30 count (NDC 59746- 758-30) & b) 90 count (NDC 59746-758-90) bottles, Rx only, Manufactured b Jubilant Generis Ltd, Roorkee, India, Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Failed Dissolution Specifications; 9-monthstability timepoint

What to do

FDA enforcement status: Terminated

Brands named

jubilant cadista pharmaceuticalsjubilantjubilant cadista

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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