Dexmedetomidine Hydrochloride 70069-0759
Product NDC
70069-0759- Manufacturer
- Somerset Therapeutics, Llc
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- September 26, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA218112
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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)
4 VIAL in 1 CARTON (70069-759-04) / 10 mL in 1 VIAL