FDA NDC Directory · JSON-LD · Markdown

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NDC 58657-231 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameGabapentin
Labeler / ManufacturerMethod Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA204989
Dosage form / routeCAPSULE · ORAL
Active ingredientsGABAPENTIN (200 mg/1)
Marketing started20260309
Package count1

External sources

Source: openFDA. Public-domain (CC0).