Fentanyl Citrate 00409-9093
Product NDC
00409-9093- Manufacturer
- Hospira, Inc.
- Dosage Form
- Injection, Solution
- Route
- Intramuscular And Intravenous
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- December 6, 2016
- Listing Expires
- December 31, 2027
- Application
- NDA019115
Active Ingredients
| Ingredient | Strength |
|---|---|
| Fentanyl Citrate | 50 ug/mL |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(1)
10 AMPULE in 1 CELLO PACK (0409-9093-11) / 2 mL in 1 AMPULE (0409-9093-09)