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GABAPENTIN

NDC 76420-836 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameGabapentin
Labeler / ManufacturerAsclemed USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214957
Dosage form / routeTABLET · ORAL
Active ingredientsGABAPENTIN (600 mg/1)
Marketing started20211001
Package count6

External sources

Source: openFDA. Public-domain (CC0).