FDA NDC Directory · JSON-LD · Markdown

GABAPENTIN

NDC 68788-7024 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090007
Dosage form / routeCAPSULE · ORAL
Active ingredientsGABAPENTIN (300 mg/1)
Marketing started20200601
Package count7

External sources

Source: openFDA. Public-domain (CC0).