FDA NDC Directory · JSON-LD · Markdown

Gabapentin

NDC 69367-345 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerWestminster Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075477
Dosage form / routeCAPSULE · ORAL
Active ingredientsGABAPENTIN (400 mg/1)
Marketing started20211101
Package count1

External sources

Source: openFDA. Public-domain (CC0).