FDA NDC Directory · JSON-LD · Markdown

Gabapentin

NDC 68382-204 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078926
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsGABAPENTIN (600 mg/1)
Marketing started20121016
Package count3

External sources

Source: openFDA. Public-domain (CC0).