FDA NDC Directory · JSON-LD · Markdown

gabapentin

NDC 50228-524 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerScieGen Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA218491
Dosage form / routeTABLET · ORAL
Active ingredientsGABAPENTIN (600 mg/1)
Marketing started20250920
Package count3

External sources

Source: openFDA. Public-domain (CC0).