FDA NDC

Neupro

This name is from the loaded FDA file.

Source: FDA NDC Directory, live from openFDA. Publisher page

NDC
50474-801
Proprietary name
Neupro
Nonproprietary name
rotigotine
Labeler
UCB, Inc.
Dosage form
PATCH, EXTENDED RELEASE
Strength
1 mg/24h

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