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Pregabalin

NDC 72888-050 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerAdvagen Pharma Ltd.
Marketing categoryAbbreviated NDA (generic) · App ANDA215249
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsPREGABALIN (165 mg/1)
Marketing started20220322
Package count1

External sources

Source: openFDA. Public-domain (CC0).