NDC 70069-758 – Dexmedetomidine Hydrochloride
Dexmedetomidine Hydrochloride 100 ug/mL · Injection, Solution · Intravenous
Product NDC70069-758
Product details
- Brand name
- Dexmedetomidine Hydrochloride
- Generic name
- Dexmedetomidine Hydrochloride
- Labeler
- Somerset Therapeutics, LLC
- Dosage form
- Injection, Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA218112
- Marketed since
- September 26, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Central alpha-2 Adrenergic Agonist
Active ingredients
- Dexmedetomidine Hydrochloride 100 ug/mL
Uses, dosage, side effects and warnings for Dexmedetomidine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 70069-758-04 | 4 VIAL in 1 CARTON (70069-758-04) / 4 mL in 1 VIAL | Sep 26, 2024 |
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