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Neupro

NDC 50474-802 · HUMAN PRESCRIPTION DRUG · PATCH, EXTENDED RELEASE

Generic namerotigotine
Labeler / ManufacturerUCB, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA021829
Dosage form / routePATCH, EXTENDED RELEASE · TRANSDERMAL
Active ingredientsROTIGOTINE (2 mg/24h)
Marketing started20120402
Package count2

External sources

Source: openFDA. Public-domain (CC0).