FDA NDC Directory · JSON-LD · Markdown

GABAPENTIN

NDC 68788-8488 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameGabapentin
Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214957
Dosage form / routeTABLET · ORAL
Active ingredientsGABAPENTIN (600 mg/1)
Marketing started20230721
Package count5

External sources

Source: openFDA. Public-domain (CC0).