NDC Code | 71872-7150-1 |
Package Description | 1 VIAL in 1 BAG (71872-7150-1) / 2 mL in 1 VIAL |
Product NDC | 71872-7150 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Dexmedetomidine |
Non-Proprietary Name | Dexmedetomidine |
Dosage Form | INJECTION, SOLUTION, CONCENTRATE |
Usage | INTRAVENOUS |
Start Marketing Date | 20180301 |
Marketing Category Name | ANDA |
Application Number | ANDA209065 |
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] |