FDA NDC Directory · JSON-LD · Markdown

Gabapentin

NDC 71205-457 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameGABAPENTIN
Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA203244
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsGABAPENTIN (600 mg/1)
Marketing started20140111
Package count3

External sources

Source: openFDA. Public-domain (CC0).