NDC 71288-505 – Dexmedetomidine
Dexmedetomidine Hydrochloride 100 ug/mL · Injection, Solution · Intravenous
Product NDC71288-505
Product details
- Brand name
- Dexmedetomidine
- Generic name
- Dexmedetomidine
- Labeler
- Meitheal Pharmaceuticals Inc.
- Dosage form
- Injection, Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA204843
- Marketed since
- January 18, 2019
- 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 →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 71288-505-03 | 25 VIAL, SINGLE-DOSE in 1 CARTON (71288-505-03) / 2 mL in 1 VIAL, SINGLE-DOSE (71288-505-02) | Jan 18, 2019 |
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