NDC Code | 71872-7031-1 |
Package Description | 1 VIAL in 1 BAG (71872-7031-1) / 2 mL in 1 VIAL |
Product NDC | 71872-7031 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Dexmedetomidine Hydrochloride |
Non-Proprietary Name | Dexmedetomidine Hydrochloride |
Dosage Form | INJECTION, SOLUTION |
Usage | INTRAVENOUS |
Start Marketing Date | 20160317 |
Marketing Category Name | ANDA |
Application Number | ANDA205867 |
Manufacturer | Medical Purchasing Solutions, LLC |
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] |