FDA NDC Directory · JSON-LD · Markdown

Gabapentin

NDC 65862-200 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA078787
Dosage form / routeCAPSULE · ORAL
Active ingredientsGABAPENTIN (400 mg/1)
Marketing started20080131
Package count5

External sources

Source: openFDA. Public-domain (CC0).