NDC Code | 45963-906-42 |
Package Description | 25 VIAL, SINGLE-DOSE in 1 CARTON (45963-906-42) > 2 mL in 1 VIAL, SINGLE-DOSE (45963-906-41) |
Product NDC | 45963-906 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Dexmedetomidine Hydrochloride |
Non-Proprietary Name | Dexmedetomidine Hydrochloride |
Dosage Form | INJECTION, SOLUTION |
Usage | INTRAVENOUS |
Start Marketing Date | 20170113 |
Marketing Category Name | ANDA |
Application Number | ANDA204686 |
Manufacturer | Actavis Pharma, Inc. |
Substance Name | DEXMEDETOMIDINE HYDROCHLORIDE |
Strength | 100 |
Strength Unit | ug/mL |
Pharmacy Classes | Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC],General Anesthesia [PE] |