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: