FDA NDC Directory · JSON-LD · Markdown

Gabapentin

NDC 71335-1007 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameGABAPENTIN
Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA203244
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsGABAPENTIN (800 mg/1)
Marketing started20140111
Package count9

External sources

Source: openFDA. Public-domain (CC0).