Fentanyl Citrate 00641-6029
Product NDC
00641-6029- Manufacturer
- Hikma Pharmaceuticals Usa Inc.
- Dosage Form
- Injection
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- July 11, 1984
- Listing Expires
- December 31, 2027
- Application
- NDA019101
Active Ingredients
| Ingredient | Strength |
|---|---|
| Fentanyl Citrate | 50 ug/mL |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(2)
20 mL in 1 VIAL (0641-6029-01)
25 VIAL in 1 CARTON (0641-6029-25) / 20 mL in 1 VIAL (0641-6029-01)