FDA NDC Directory · JSON-LD · Markdown

Neurontin

NDC 0071-0401 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namegabapentin
Labeler / ManufacturerParke-Davis Div of Pfizer Inc
Marketing categoryNew Drug Application (innovator) · App NDA020882
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsGABAPENTIN (800 mg/1)
Marketing started19981009
Marketing ended20260731
Package count1

External sources

Source: openFDA. Public-domain (CC0).