Fentanyl Citrate 81565-0205
Product NDC
81565-0205- Manufacturer
- Phlow Corp.
- Dosage Form
- Injection
- Route
- Intramuscular And Intravenous
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- January 11, 2023
- Application
- NDA019101
Active Ingredients
| Ingredient | Strength |
|---|---|
| Fentanyl Citrate | 50 ug/mL |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(1)
25 VIAL in 1 CARTON (81565-205-02) / 2 mL in 1 VIAL (81565-205-01)