Desmopressin acetate (Teva Parenteral Medicines, Inc.)
Welcome to the PulseAid listing for the Desmopressin acetate drug offered from Teva Parenteral Medicines, Inc.. 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: | Teva Parenteral Medicines, Inc. |
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: | INTRAVENOUS |
DOSAGE FORM: | INJECTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 1997-11-01 |
END MARKETING DATE: | 0000-00-00 |
Desmopressin acetate HUMAN PRESCRIPTION DRUG Details:
Item Description | Desmopressin acetate from Teva Parenteral Medicines, Inc. |
LABELER NAME: | Teva Parenteral Medicines, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 4(ug/mL) |
START MARKETING DATE: | 1997-11-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0703-5051_ff87d1d1-98e4-42d0-afba-34cd1a7f2b2e |
PRODUCT NDC: | 0703-5051 |
APPLICATION NUMBER: | ANDA074888 |
Other DESMOPRESSIN ACETATE Pharmaceutical Manufacturers / Labelers: