Desmopressin Acetate (Sun Pharma Global FZE)
Welcome to the PulseAid listing for the Desmopressin Acetate drug offered from Sun Pharma Global FZE. This Factor VIII Activator [EPC],Increased Coagulation Factor VIII Activity [PE],Increased Coagulation Factor VIII Concentration [PE],Vasopressin Analog [EPC],Vasopressins [Chemical/Ingredient] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Sun Pharma Global FZE |
| NON-PROPRIETARY NAME: | Desmopressin Acetate |
| SUBSTANCE NAME: | DESMOPRESSIN ACETATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Factor VIII Activator [EPC],Increased Coagulation Factor VIII Activity [PE],Increased Coagulation Factor VIII Concentration [PE],Vasopressin Analog [EPC],Vasopressins [Chemical/Ingredient] |
| ROUTE: | NASAL |
| DOSAGE FORM: | SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2013-12-24 |
| END MARKETING DATE: | 0000-00-00 |
Desmopressin Acetate HUMAN PRESCRIPTION DRUG Details:
| Item Description | Desmopressin Acetate from Sun Pharma Global FZE |
| LABELER NAME: | Sun Pharma Global FZE |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 0.1(mg/mL) |
| START MARKETING DATE: | 2013-12-24 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 47335-788_65420316-3251-490b-a0ef-e4cfec5cc384 |
| PRODUCT NDC: | 47335-788 |
| APPLICATION NUMBER: | ANDA078271 |
Other DESMOPRESSIN ACETATE Pharmaceutical Manufacturers / Labelers:
