Dexmedetomidine Hydrochloride 57664-0596
Product NDC
57664-0596- Manufacturer
- Sun Pharmaceuticals Industries, Inc.
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- April 8, 2015
- Listing Expires
- December 31, 2026
- Application
- ANDA202126
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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, SINGLE-DOSE in 1 CARTON (57664-596-50) / 2 mL in 1 VIAL, SINGLE-DOSE (57664-596-40)