Key Takeaway

Paroxetine Extended-Release Tablets USP, 12.5 mg, 30 count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland, 21202, Manufactured by: Lupin Limited, Pithampur (M.P.) 4 by Lupin Pharmaceuticals Inc. was recalled on June 22, 2017. The hazard: Failed Dissolution Specifications: out of specification observed in dissolution testing at 3 month long term stability study.

FDA Drug Class III Terminated

Paroxetine Extended-Release Tablets USP, 12.5 mg, 30 count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland, 21202, Manufactured by: Lupin Limited, Pithampur (M.P.) 4

Recalled: June 22, 2017 ~12480 bottles units affected D-0974-2017

Description

Paroxetine Extended-Release Tablets USP, 12.5 mg, 30 count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland, 21202, Manufactured by: Lupin Limited, Pithampur (M.P.) 454 775, India, NDC: 68180-647-06

Hazard / Reason

Failed Dissolution Specifications: out of specification observed in dissolution testing at 3 month long term stability study.

Class III: Product that is not likely to cause adverse health consequences.

Class III is the least severe classification. The product is unlikely to cause adverse health consequences but still violates FDA regulations.

Products Affected

Paroxetine Extended-Release Tablets USP, 12.5 mg, 30 count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland, 21202, Manufactured by: Lupin Limited, Pithampur (M.P.) 4

Drugs

Company Information

Lupin Pharmaceuticals Inc.

Baltimore, MD, United States

View all 119 recalls by Lupin Pharmaceuticals Inc. →

Distribution

Nationwide in the USA

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