United States · FDA National Drug Code directory
FENTANYL
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
- 50742-552_4edfd739-fc61-0f08-e063-6394a90ae646
- Product NDC
- 50742-552
- Form
- PATCH, EXTENDED RELEASE
- Composition / generic term
- FENTANYL
- Labeler
- INGENUS PHARMACEUTICALS, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250106
- Source listing expiry
- 20271231
Source-listed ingredients
- FENTANYL — 50 ug/h
These values do not establish equivalence or a dose recommendation.
Packages
- 5 POUCH in 1 CARTON (50742-552-05) / 1 PATCH in 1 POUCH (50742-552-01) / 72 h in 1 PATCH · 50742-552-05
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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