Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride 00781-3494
Product NDC
00781-3494- Manufacturer
- Sandoz Inc.
- Dosage Form
- Injection
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- June 12, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA209065
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Dexmedetomidine Hydrochloride | 4 ug/mL |
Drug Class
Adrenergic alpha2-Agonists [MoA]Central alpha-2 Adrenergic Agonist [EPC]General Anesthesia [PE]
Packaging Options(1)
10 BOTTLE in 1 CARTON (0781-3494-95) / 50 mL in 1 BOTTLE
External Resources