FDA NDC Directory · JSON-LD · Markdown

GABAPENTIN

NDC 82804-249 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameGabapentin
Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA214957
Dosage form / routeTABLET · ORAL
Active ingredientsGABAPENTIN (800 mg/1)
Marketing started20211001
Package count1

External sources

Source: openFDA. Public-domain (CC0).