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Anticonvulsant Recalled
12/27/2019
The recall affects 100-mg gabapentin capsules (NDC 65682-198-99) from lot 19819029A3 (Exp. 8/21). The product was distributed throughout the United States.
AuroMedics Pharma initiated the voluntary recall November 19, 2019. At press time, the FDA had not yet classified the recall.
Gabapentin is a prescription anticonvulsant used to treat seizures as well as nerve pain associated with shingles.
—Jolynn Tumolo