NDC 70121-1388 – Dexmedetomidine Hydrochloride
Dexmedetomidine Hydrochloride 4 ug/mL · Injection, Solution · Intravenous
Product NDC70121-1388
Product details
- Brand name
- Dexmedetomidine Hydrochloride
- Generic name
- Dexmedetomidine Hydrochloride
- Labeler
- Amneal Pharmaceuticals LLC
- Dosage form
- Injection, Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA207551
- Marketed since
- May 20, 2020
- Listing expires
- December 31, 2027
- Pharmacologic class
- Central alpha-2 Adrenergic Agonist
Active ingredients
- Dexmedetomidine Hydrochloride 4 ug/mL
Uses, dosage, side effects and warnings for Dexmedetomidine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 70121-1388-8 | 20 BOTTLE, GLASS in 1 CARTON (70121-1388-8) / 50 mL in 1 BOTTLE, GLASS (70121-1388-1) | May 20, 2020 |
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