NDC 36000-262 – Dexmedetomidine Hydrochloride
Dexmedetomidine Hydrochloride 100 ug/mL · Injection, Solution, Concentrate · Intravenous
Product NDC36000-262
Product details
- Brand name
- Dexmedetomidine Hydrochloride
- Generic name
- Dexmedetomidine hydrochloride
- Labeler
- Baxter Healthcare Corporation
- Dosage form
- Injection, Solution, Concentrate
- Route
- Intravenous
- Marketing category
- ANDA · ANDA208103
- Marketed since
- April 16, 2026
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 36000-262-05 | 5 VIAL, SINGLE-DOSE in 1 CARTON (36000-262-05) / 2 mL in 1 VIAL, SINGLE-DOSE (36000-262-01) | Apr 16, 2026 |
| 36000-262-10 | 10 VIAL, SINGLE-DOSE in 1 CARTON (36000-262-10) / 2 mL in 1 VIAL, SINGLE-DOSE (36000-262-01) | Apr 16, 2026 |
| 36000-262-25 | 25 VIAL, SINGLE-DOSE in 1 CARTON (36000-262-25) / 2 mL in 1 VIAL, SINGLE-DOSE (36000-262-01) | Apr 16, 2026 |
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