| NDC Code | 47335-788-91 |
|---|
| Package Description | 1 BOTTLE, SPRAY in 1 CARTON (47335-788-91) > 5 mL in 1 BOTTLE, SPRAY |
|---|
| Product NDC | 47335-788 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Desmopressin Acetate |
|---|
| Non-Proprietary Name | Desmopressin Acetate |
|---|
| Dosage Form | SOLUTION |
|---|
| Usage | NASAL |
|---|
| Start Marketing Date | 20131224 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078271 |
|---|
| Manufacturer | Sun Pharmaceutical Industries, Inc. |
|---|
| Substance Name | DESMOPRESSIN ACETATE |
|---|
| Strength | .1 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Factor VIII Activator [EPC], Increased Coagulation Factor VIII Activity [PE], Increased Coagulation Factor VIII Concentration [PE], Vasopressin Analog [EPC], Vasopressins [CS] |
|---|