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Desmopressin Acetate
Desmopressin Acetate - 55566-5040-1 - (desmopressin acetate)
Drug Information of Desmopressin Acetate
| Product NDC: | 55566-5040 |
| Proprietary Name: | Desmopressin Acetate |
| Non Proprietary Name: | desmopressin acetate |
| Active Ingredient(s): | 4 ug/mL & nbsp; desmopressin acetate |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Desmopressin Acetate
| Product NDC: | 55566-5040 |
| Labeler Name: | Ferring Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018938 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19991026 |
Package Information of Desmopressin Acetate
| Package NDC: | 55566-5040-1 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (55566-5040-1) > 10 mL in 1 VIAL, MULTI-DOSE (55566-5040-0) |
NDC Information of Desmopressin Acetate
| NDC Code | 55566-5040-1 |
| Proprietary Name | Desmopressin Acetate |
| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (55566-5040-1) > 10 mL in 1 VIAL, MULTI-DOSE (55566-5040-0) |
| Product NDC | 55566-5040 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | desmopressin acetate |
| Dosage Form Name | SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19991026 |
| Marketing Category Name | NDA |
| Labeler Name | Ferring Pharmaceuticals Inc. |
| Substance Name | DESMOPRESSIN ACETATE |
| Strength Number | 4 |
| Strength Unit | ug/mL |
| Pharmaceutical Classes | Factor VIII Activator [EPC],Increased Coagulation Factor VIII Activity [PE],Increased Coagulation Factor VIII Concentration [PE],Vasopressin Analog [EPC],Vasopressins [Chemical/Ingredient] |
