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Neupro

NDC 50474-805, rotigotine, patch, extended release, from UCB, Inc..

Product NDC
50474-805
Status
Listed
Labeler
UCB, Inc.
Dosage form
PATCH, EXTENDED RELEASE
Route
TRANSDERMAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA021829
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50474-805 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ROTIGOTINE6 mg/24h

Pharmacologic classes

Dopamine Agonists [MoA]; Nonergot Dopamine Agonist [EPC]

Package NDCNDC-11Package
50474-805-035047408050330 POUCH in 1 CARTON (50474-805-03) / 1 PATCH in 1 POUCH / 24 h in 1 PATCH
50474-805-17504740805177 POUCH in 1 CARTON (50474-805-17) / 1 PATCH in 1 POUCH / 24 h in 1 PATCH

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/939e28c5-f3a9-42c0-9a2d-8d471d82a6e0

  • NADAC price for package 50474080503

    GET /v1/drugs/nadac/50474080503

Use it

Look up 50474-805 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50474-805 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50474-805. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.