| NDC Code | 42023-146-25 |
|---|
| Package Description | 25 VIAL in 1 CARTON (42023-146-25) / 2 mL in 1 VIAL |
|---|
| Product NDC | 42023-146 |
|---|
| 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 | 20140819 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA203972 |
|---|
| Manufacturer | ENDO USA, 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] |
|---|