FDA NDC Directory · JSON-LD · Markdown

Gabapentin

NDC 72189-471 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerDirect_Rx
Marketing categoryAbbreviated NDA (generic) · App ANDA214957
Dosage form / routeTABLET · ORAL
Active ingredientsGABAPENTIN (600 mg/1)
Marketing started20230515
Package count4

External sources

Source: openFDA. Public-domain (CC0).