Neupro
NDC 50474-808, rotigotine, kit, from UCB, Inc..
- Product NDC
- 50474-808
- Status
- Listed
- Labeler
- UCB, Inc.
- Dosage form
- KIT
- Route
- —
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA021829
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/50474-808 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
None listed.
| Package NDC | NDC-11 | Package |
|---|---|---|
| 50474-808-11 | 50474080811 | 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 |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/939e28c5-f3a9-42c0-9a2d-8d471d82a6e0
Use it
Look up 50474-808 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/50474-808 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 50474-808. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.