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DESMOPRESSIN ACETATE
DESMOPRESSIN ACETATE - 60505-0815-0 - (DESMOPRESSIN ACETATE)
Drug Information of DESMOPRESSIN ACETATE
| Product NDC: | 60505-0815 |
| Proprietary Name: | DESMOPRESSIN ACETATE |
| Non Proprietary Name: | DESMOPRESSIN ACETATE |
| Active Ingredient(s): | 10 ug/1 & nbsp; DESMOPRESSIN ACETATE |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DESMOPRESSIN ACETATE
| Product NDC: | 60505-0815 |
| Labeler Name: | Apotex Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076703 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050127 |
Package Information of DESMOPRESSIN ACETATE
| Package NDC: | 60505-0815-0 |
| Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (60505-0815-0) > 50 SPRAY in 1 BOTTLE, SPRAY |
NDC Information of DESMOPRESSIN ACETATE
| NDC Code | 60505-0815-0 |
| Proprietary Name | DESMOPRESSIN ACETATE |
| Package Description | 1 BOTTLE, SPRAY in 1 CARTON (60505-0815-0) > 50 SPRAY in 1 BOTTLE, SPRAY |
| Product NDC | 60505-0815 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DESMOPRESSIN ACETATE |
| Dosage Form Name | SPRAY |
| Route Name | NASAL |
| Start Marketing Date | 20050127 |
| Marketing Category Name | ANDA |
| Labeler Name | Apotex Corp. |
| Substance Name | DESMOPRESSIN ACETATE |
| Strength Number | 10 |
| Strength Unit | ug/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] |
