NDC 50742-555 – Fentanyl

Fentanyl 87.5 ug/h · Patch, Extended Release · Transdermal

Human Prescription Drug DEA schedule CII

Product NDC50742-555

Product details

Brand name
Fentanyl
Generic name
Fentanyl
Labeler
INGENUS PHARMACEUTICALS, LLC
Dosage form
Patch, Extended Release
Route
Transdermal
Marketing category
ANDA · ANDA077449
Marketed since
February 11, 2025
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Fentanyl →

Package NDC codes (1)

Package NDCDescriptionSince
50742-555-055 POUCH in 1 CARTON (50742-555-05) / 1 PATCH in 1 POUCH (50742-555-01) / 72 h in 1 PATCHFeb 11, 2025

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