FDAJune 29, 2020drug

Carbamazepine 200 mg Tablets, 100-unit dose tablets per box, Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC 70518-2489-00 for box; 70518-2489-01 per unit dose.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

FAILED DISSOLUTION SPECIFICATION: Low out-of-specification (OOS) dissolution results obtained during routine stability testing.

What to do

FDA enforcement status: Terminated

Brands named

remedyrepack

UPCs

7051824890070518248901

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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