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GABAPENTIN

NDC 23155-866 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic namegabapentin
Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211314
Dosage form / routeCAPSULE · ORAL
Active ingredientsGABAPENTIN (100 mg/1)
Marketing started20230625
Marketing ended20261231
Package count2

External sources

Source: openFDA. Public-domain (CC0).