Dexmedetomidine Hydrochloride 65219-0642
Product NDC
65219-0642- Manufacturer
- Fresenius Kabi Usa, Llc
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- September 18, 2015
- Listing Expires
- December 31, 2027
- Application
- ANDA201072
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Dexmedetomidine Hydrochloride | 100 ug/mL |
Drug Class
Adrenergic alpha2-Agonists [MoA]Central alpha-2 Adrenergic Agonist [EPC]General Anesthesia [PE]
Packaging Options(1)
25 VIAL in 1 TRAY (65219-642-02) / 2 mL in 1 VIAL (65219-642-01)