FDA NDC Directory · JSON-LD · Markdown

Gabapentin

NDC 42385-979 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerLaurus Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA217965
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsGABAPENTIN (600 mg/1)
Marketing started20240409
Package count6

External sources

Source: openFDA. Public-domain (CC0).