World Of Taxonomy
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]

GET/api/v1/systems/ndc_fda/nodes/50474-801
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