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Desmopressin Acetate
Desmopressin Acetate - 68084-606-21 - (Desmopressin Acetate)
Drug Information of Desmopressin Acetate
| Product NDC: | 68084-606 |
| 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: | 68084-606 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076470 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121008 |
Package Information of Desmopressin Acetate
| Package NDC: | 68084-606-21 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (68084-606-21) > 10 TABLET in 1 BLISTER PACK (68084-606-11) |
NDC Information of Desmopressin Acetate
| NDC Code | 68084-606-21 |
| Proprietary Name | Desmopressin Acetate |
| Package Description | 3 BLISTER PACK in 1 CARTON (68084-606-21) > 10 TABLET in 1 BLISTER PACK (68084-606-11) |
| Product NDC | 68084-606 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Desmopressin Acetate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20121008 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| 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] |
