FDA NDC Directory · JSON-LD · Markdown

gabapentin

NDC 68382-356 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203934
Dosage form / routeTABLET · ORAL
Active ingredientsGABAPENTIN (750 mg/1)
Marketing started20250918
Package count2

External sources

Source: openFDA. Public-domain (CC0).