FDA NDC Directory · JSON-LD · Markdown

Gabapentin

NDC 65862-523 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA200651
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsGABAPENTIN (600 mg/1)
Marketing started20111006
Package count4

External sources

Source: openFDA. Public-domain (CC0).