| NDC Code | 36000-262-25 |
|---|
| Package Description | 25 VIAL, SINGLE-DOSE in 1 CARTON (36000-262-25) / 2 mL in 1 VIAL, SINGLE-DOSE (36000-262-01) |
|---|
| Product NDC | 36000-262 |
|---|
| 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 | 20260416 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA208103 |
|---|
| Manufacturer | Baxter Healthcare Corporation |
|---|
| 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] |
|---|