FDA NDC Directory · JSON-LD · Markdown

Gabapentin

NDC 50268-326 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerAvPAK
Marketing categoryAbbreviated NDA (generic) · App ANDA207057
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsGABAPENTIN (800 mg/1)
Marketing started20230808
Package count1

External sources

Source: openFDA. Public-domain (CC0).