FDA NDC Directory · JSON-LD · Markdown

GABAPENTIN

NDC 72189-158 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerDIRECT RX
Marketing categoryAbbreviated NDA (generic) · App ANDA203244
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsGABAPENTIN (800 mg/1)
Marketing started20201201
Package count4

External sources

Source: openFDA. Public-domain (CC0).