| NDC Code | 39822-6200-2 |
|---|
| Package Description | 10 VIAL in 1 CARTON (39822-6200-2) / 1 mL in 1 VIAL (39822-6200-1) |
|---|
| Product NDC | 39822-6200 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Desmopressin Acetate |
|---|
| Non-Proprietary Name | Desmopressin Acetate |
|---|
| Dosage Form | INJECTION, SOLUTION |
|---|
| Usage | INTRAVENOUS; SUBCUTANEOUS |
|---|
| Start Marketing Date | 20240322 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA210223 |
|---|
| Manufacturer | XGen Pharmaceuticals DJB, Inc. |
|---|
| Substance Name | DESMOPRESSIN ACETATE |
|---|
| Strength | 4 |
|---|
| Strength Unit | ug/mL |
|---|
| Pharmacy Classes | Factor VIII Activator [EPC], Increased Coagulation Factor VIII Activity [PE], Increased Coagulation Factor VIII Concentration [PE], Vasopressin Analog [EPC], Vasopressins [CS] |
|---|