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Gabapentin

NDC 71610-044 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameGABAPENTIN
Labeler / ManufacturerAphena Pharma Solutions - Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA203244
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsGABAPENTIN (600 mg/1)
Marketing started20140111
Package count8

External sources

Source: openFDA. Public-domain (CC0).