FDA NDC Directory · JSON-LD · Markdown

Gabapentin

NDC 17856-0600 · HUMAN PRESCRIPTION DRUG · SOLUTION

Generic namegabapentin
Labeler / ManufacturerATLANTIC BIOLOGICALS CORP.
Marketing categoryAbbreviated NDA (generic) · App ANDA076403
Dosage form / routeSOLUTION · ORAL
Active ingredientsGABAPENTIN (250 mg/5mL)
Marketing started20180629
Package count4

External sources

Source: openFDA. Public-domain (CC0).