NDC 57664-596 – Dexmedetomidine Hydrochloride
Dexmedetomidine Hydrochloride 100 ug/mL · Injection, Solution · Intravenous
Product NDC57664-596
Product details
- Brand name
- Dexmedetomidine Hydrochloride
- Generic name
- Dexmedetomidine Hydrochloride
- Labeler
- Sun Pharmaceuticals Industries, Inc.
- Dosage form
- Injection, Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA202126
- Marketed since
- April 8, 2015
- 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 |
|---|---|---|
| 57664-596-50 | 25 VIAL, SINGLE-DOSE in 1 CARTON (57664-596-50) / 2 mL in 1 VIAL, SINGLE-DOSE (57664-596-40) | Apr 8, 2015 |
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