United States · FDA National Drug Code directory
Neupro
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 50474-808_5b24ae50-a285-526a-e063-6294a90a9998
- Product NDC
- 50474-808
- Form
- KIT
- Composition / generic term
- rotigotine
- Labeler
- UCB, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20120402
- Source listing expiry
- 20271231
Source-listed ingredients
Separate ingredient quantities are not available in this snapshot. Any composition term above is preserved as source text.
These values do not establish equivalence or a dose recommendation.
Packages
- 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 · 50474-808-11
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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