NDC 65219-642 – Dexmedetomidine Hydrochloride
Dexmedetomidine Hydrochloride 100 ug/mL · Injection, Solution · Intravenous
Product NDC65219-642
Product details
- Brand name
- Dexmedetomidine Hydrochloride
- Generic name
- dexmedetomidine hydrochloride
- Labeler
- Fresenius Kabi USA, LLC
- Dosage form
- Injection, Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA201072
- Marketed since
- September 18, 2015
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 65219-642-02 | 25 VIAL in 1 TRAY (65219-642-02) / 2 mL in 1 VIAL (65219-642-01) | Dec 13, 2024 |
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