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Desmopressin Acetate
Desmopressin Acetate - 0093-7316-01 - (Desmopressin Acetate)
Drug Information of Desmopressin Acetate
| Product NDC: | 0093-7316 |
| Proprietary Name: | Desmopressin Acetate |
| Non Proprietary Name: | Desmopressin Acetate |
| Active Ingredient(s): | .1 mg/1 & nbsp; Desmopressin Acetate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Desmopressin Acetate
| Product NDC: | 0093-7316 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077122 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060127 |
Package Information of Desmopressin Acetate
| Package NDC: | 0093-7316-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0093-7316-01) |
NDC Information of Desmopressin Acetate
| NDC Code | 0093-7316-01 |
| Proprietary Name | Desmopressin Acetate |
| Package Description | 100 TABLET in 1 BOTTLE (0093-7316-01) |
| Product NDC | 0093-7316 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Desmopressin Acetate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20060127 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | DESMOPRESSIN ACETATE |
| Strength Number | .1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Factor VIII Activator [EPC],Increased Coagulation Factor VIII Activity [PE],Increased Coagulation Factor VIII Concentration [PE],Vasopressin Analog [EPC],Vasopressins [Chemical/Ingredient] |
