Fentanyl 50742-0549
Product NDC
50742-0549- Manufacturer
- Ingenus Pharmaceuticals, Llc
- Dosage Form
- Patch, Extended Release
- Route
- Transdermal
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- January 30, 2025
- Listing Expires
- December 31, 2027
- Application
- ANDA077449
Active Ingredients
| Ingredient | Strength |
|---|---|
| Fentanyl | 12 ug/h |
Drug Class
Opioid Agonist [EPC]Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(1)
5 POUCH in 1 CARTON (50742-549-05) / 1 PATCH in 1 POUCH (50742-549-01) / 72 h in 1 PATCH