FDA NDC Directory · JSON-LD · Markdown

Gabapentin

NDC 82804-015 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA205101
Dosage form / routeTABLET · ORAL
Active ingredientsGABAPENTIN (600 mg/1)
Marketing started20160411
Package count3

External sources

Source: openFDA. Public-domain (CC0).