NDC 70121-1712 – Dexmedetomidine Hydrochloride
Dexmedetomidine Hydrochloride 4 ug/mL · Injection · Intravenous
Product NDC70121-1712
Product details
- Brand name
- Dexmedetomidine Hydrochloride
- Generic name
- Dexmedetomidine Hydrochloride in Sodium Chloride
- Labeler
- Amneal Pharmaceuticals LLC
- Dosage form
- Injection
- Route
- Intravenous
- Marketing category
- ANDA · ANDA216604
- Marketed since
- May 19, 2023
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 70121-1712-2 | 10 POUCH in 1 CARTON (70121-1712-2) / 1 BAG in 1 POUCH / 100 mL in 1 BAG | Jan 8, 2024 |
| 70121-1712-3 | 12 POUCH in 1 CARTON (70121-1712-3) / 1 BAG in 1 POUCH / 100 mL in 1 BAG | May 19, 2023 |
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