NDC Code | 67457-580-02 |
Package Description | 25 VIAL, GLASS in 1 CARTON (67457-580-02) > 2 mL in 1 VIAL, GLASS (67457-580-00) |
Product NDC | 67457-580 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Dexmedetomidine Hydrochloride |
Non-Proprietary Name | Dexmedetomidine Hydrochloride |
Dosage Form | INJECTION, SOLUTION, CONCENTRATE |
Usage | INTRAVENOUS |
Start Marketing Date | 20150609 |
End Marketing Date | 20170731 |
Marketing Category Name | ANDA |
Application Number | ANDA202881 |
Manufacturer | Mylan Institutional 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] |