Key Takeaway

DIVALPROEX SODIUM EXTENDED-RELEASE TABLETS, USP Tablets, 250 mg, 100 count-unit dose carton, RX only, Manufactured by Dr. Reddy's Laboratories Ltd. Bachupally - 500 090 India. Distributed by: Major Ph by MAJOR PHARMACEUTICALS was recalled on April 24, 2019. The hazard: cGMP deviations: Product was exposed above 50% relative humidity levels during packaging operations.

FDA Drug Class II Terminated

DIVALPROEX SODIUM EXTENDED-RELEASE TABLETS, USP Tablets, 250 mg, 100 count-unit dose carton, RX only, Manufactured by Dr. Reddy's Laboratories Ltd. Bachupally - 500 090 India. Distributed by: Major Ph

Recalled: April 24, 2019 ~828 100-count unit dose cartons units affected D-1583-2019

Description

DIVALPROEX SODIUM EXTENDED-RELEASE TABLETS, USP Tablets, 250 mg, 100 count-unit dose carton, RX only, Manufactured by Dr. Reddy's Laboratories Ltd. Bachupally - 500 090 India. Distributed by: Major Pharmaceuticals 17177 N Laurel Park Dr., Suite 233 Livonia, MI 48152. NDC # 0904-6363-61.

Hazard / Reason

cGMP deviations: Product was exposed above 50% relative humidity levels during packaging operations.

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

DIVALPROEX SODIUM EXTENDED-RELEASE TABLETS, USP Tablets, 250 mg, 100 count-unit dose carton, RX only, Manufactured by Dr. Reddy's Laboratories Ltd. Bachupally - 500 090 India. Distributed by: Major Ph

Drugs

Company Information

MAJOR PHARMACEUTICALS

Livonia, MI, United States

View all 7 recalls by MAJOR PHARMACEUTICALS →

Distribution

Nationwide in the USA

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