| NDC Code | 43598-976-58 |
|---|
| Package Description | 10 VIAL in 1 CARTON (43598-976-58) > 50 mL in 1 VIAL (43598-976-11) |
|---|
| Product NDC | 43598-976 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Dexmedetomidine Hydrochloride |
|---|
| Non-Proprietary Name | Dexmedetomidine Hydrochloride |
|---|
| Dosage Form | INJECTION, SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20200817 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA209307 |
|---|
| Manufacturer | Dr.Reddy's Laboratories Inc |
|---|
| Substance Name | DEXMEDETOMIDINE HYDROCHLORIDE |
|---|
| Strength | 4 |
|---|
| Strength Unit | ug/mL |
|---|
| Pharmacy Classes | Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC], General Anesthesia [PE] |
|---|