50474-808 : Neupro Kit
| NDC: | 50474-808 |
| Labeler: | Ucb, Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Neupro |
| Dosage Form: | Kit |
| Application #: | NDA021829 |
| Rev. Date: |
NDC Package Codes:
- 50474-808-11: 2 BOX IN 1 KIT (50474‑808‑11) > 1 KIT IN 1 BOX * 7 POUCH IN 1 BOX > 1 PATCH IN 1 POUCH > 24 H IN 1 PATCH * 7 POUCH IN 1 BOX > 1 PATCH IN 1 POUCH > 24 H IN 1 PATCH
Active Ingredients:
- Rotigotine
Related Products:
Based on records with the same trade name.- 50474-801 Neupro 1 mg/24h Transdermal Patch, Extended Release by Ucb, Inc.
- 50474-802 Neupro 2 mg/24h Transdermal Patch, Extended Release by Ucb, Inc.
- 50474-803 Neupro 3 mg/24h Transdermal Patch, Extended Release by Ucb, Inc.
- 50474-804 Neupro 4 mg/24h Transdermal Patch, Extended Release by Ucb, Inc.
- 50474-805 Neupro 6 mg/24h Transdermal Patch, Extended Release by Ucb, Inc.
- 50474-806 Neupro 8 mg/24h Transdermal Patch, Extended Release by Ucb, Inc.
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.