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Pregabalin Extended Release

NDC 50228-462 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic namePREGABALIN
Labeler / ManufacturerScieGen Pharmaceuticals, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA215675
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsPREGABALIN (82.5 mg/1)
Marketing started20220914
Package count2

External sources

Source: openFDA. Public-domain (CC0).