Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

BuPROPion Hydrochloride Extended-Release Tablets Recalled by Jubilant Cadista Pharmaceuticals, Inc. Due to Failed Dissolution Specifications; 9-monthstability timepoint

Date: February 28, 2019
Company: Jubilant Cadista Pharmaceuticals, Inc.
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Jubilant Cadista Pharmaceuticals, Inc. directly.

Affected Products

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

Quantity: a) 3,072 bottles; b) 2,688 bottles

Why Was This Recalled?

Failed Dissolution Specifications; 9-monthstability timepoint

Where Was This Sold?

Product was distributed to one customer who may have further distributed the product.

About Jubilant Cadista Pharmaceuticals, Inc.

Jubilant Cadista Pharmaceuticals, Inc. has 29 total recalls tracked by RecallDetector.

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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report