Key Takeaway

Clozapine Orally Disintegrating Tablets, 12.5 mg, 100-count bottles, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0093-5416-01 Yellow, round, flat-faced, beveled-edge, unscore by Teva Pharmaceuticals USA was recalled on September 21, 2018. The hazard: Failed Disintegration Specifications: Out-of-specification disintegration test result obtained during routine stability testing.

FDA Drug Class II Terminated

Clozapine Orally Disintegrating Tablets, 12.5 mg, 100-count bottles, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0093-5416-01 Yellow, round, flat-faced, beveled-edge, unscore

Recalled: September 21, 2018 ~313 bottles units affected D-0001-2019

Description

Clozapine Orally Disintegrating Tablets, 12.5 mg, 100-count bottles, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0093-5416-01 Yellow, round, flat-faced, beveled-edge, unscored tablet. Debossed with 13 on one side and plain on the other side.

Hazard / Reason

Failed Disintegration Specifications: Out-of-specification disintegration test result obtained during routine stability testing.

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

Clozapine Orally Disintegrating Tablets, 12.5 mg, 100-count bottles, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0093-5416-01 Yellow, round, flat-faced, beveled-edge, unscore

Drugs

Company Information

Teva Pharmaceuticals USA

Horsham, PA, United States

View all 196 recalls by Teva Pharmaceuticals USA →

Distribution

Distributed nationwide in the USA

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Frequently Asked Questions

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