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Desmopressin Acetate
Desmopressin Acetate - 0409-2265-01 - (Desmopressin Acetate)
Drug Information of Desmopressin Acetate
| Product NDC: | 0409-2265 |
| Proprietary Name: | Desmopressin Acetate |
| Non Proprietary Name: | Desmopressin Acetate |
| Active Ingredient(s): | 4 ug/mL & nbsp; Desmopressin Acetate |
| Administration Route(s): | INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Desmopressin Acetate
| Product NDC: | 0409-2265 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075220 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101019 |
Package Information of Desmopressin Acetate
| Package NDC: | 0409-2265-01 |
| Package Description: | 10 AMPULE in 1 BOX (0409-2265-01) > 1 mL in 1 AMPULE |
NDC Information of Desmopressin Acetate
| NDC Code | 0409-2265-01 |
| Proprietary Name | Desmopressin Acetate |
| Package Description | 10 AMPULE in 1 BOX (0409-2265-01) > 1 mL in 1 AMPULE |
| Product NDC | 0409-2265 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Desmopressin Acetate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 20101019 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, 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] |
