FDA NDC Directory · JSON-LD · Markdown

GABAPENTIN

NDC 83008-063 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameGabapentin
Labeler / ManufacturerQuality Care Products, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA214957
Dosage form / routeTABLET · ORAL
Active ingredientsGABAPENTIN (600 mg/1)
Marketing started20240610
Marketing ended20260630
Package count2

External sources

Source: openFDA. Public-domain (CC0).