NDC Code | 71872-7122-1 |
Package Description | 1 VIAL, SINGLE-DOSE in 1 BAG (71872-7122-1) / 2 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 71872-7122 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Dexmedetomidine Hydrochloride |
Non-Proprietary Name | Dexmedetomidine Hydrochloride |
Dosage Form | INJECTION, SOLUTION |
Usage | INTRAVENOUS |
Start Marketing Date | 20150408 |
Marketing Category Name | ANDA |
Application Number | ANDA202126 |
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] |