50474-801Level 3
Neupro (rotigotine)
**Product type:** Human Prescription Drug
**Active ingredient:** ROTIGOTINE
**Strength:** 1 mg/24h
**Dosage form:** Patch, Extended Release
**Route:** Transdermal
**Labeler:** UCB, Inc.
**Marketing category:** NDA (NDA021829)
**Pharmacologic class:** Dopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC]
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