Key Takeaway

Levetiracetam, extended release tablets, 750 mg, 60-count bottle, Rx only, Manufactured by Sun Pharmaceutical Ind. Ltd Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC Number: 47335-576-86 by Sun Pharma Global Fze was recalled on January 21, 2015. The hazard: Failed Dissolution Specifications: 6 month time point.

FDA Drug Class II Terminated

Levetiracetam, extended release tablets, 750 mg, 60-count bottle, Rx only, Manufactured by Sun Pharmaceutical Ind. Ltd Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC Number: 47335-576-86

Recalled: January 21, 2015 ~3263 bottles units affected D-0386-2015

Description

Levetiracetam, extended release tablets, 750 mg, 60-count bottle, Rx only, Manufactured by Sun Pharmaceutical Ind. Ltd Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC Number: 47335-576-86

Hazard / Reason

Failed Dissolution Specifications: 6 month time point.

Class II: Product that may cause temporary or medically reversible health consequences.

Class II indicates the product may cause temporary or medically reversible health effects. The probability of serious harm is considered remote.

Products Affected

Levetiracetam, extended release tablets, 750 mg, 60-count bottle, Rx only, Manufactured by Sun Pharmaceutical Ind. Ltd Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC Number: 47335-576-86

Drugs

Company Information

Sun Pharma Global Fze

Sharm, United Arab Emirates

View all 4 recalls by Sun Pharma Global Fze →

Distribution

Nationwide.

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Frequently Asked Questions

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