Dexmedetomidine Hydrochloride 71225-0133
Product NDC
71225-0133- Manufacturer
- Slayback Pharma Llc
- Dosage Form
- Injection
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- October 20, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA212791
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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)
8 BOTTLE in 1 CARTON (71225-133-02) / 100 mL in 1 BOTTLE (71225-133-01)