Duavee (Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc.)


Welcome to the PulseAid listing for the Duavee drug offered from Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc.. This Estrogen [EPC],Estrogen Receptor Agonists [MoA],Estrogens, Conjugated (USP) [Chemical/Ingredient],Estrogen Agonist/Antagonist [EPC],Selective Estrogen Receptor Modulators [MoA] 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: Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc.
NON-PROPRIETARY NAME: conjugated estrogens/bazedoxifene
SUBSTANCE NAME: ESTROGENS, CONJUGATED; BAZEDOXIFENE ACETATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Estrogen [EPC],Estrogen Receptor Agonists [MoA],Estrogens, Conjugated (USP) [Chemical/Ingredient],Estrogen Agonist/Antagonist [EPC],Selective Estrogen Receptor Modulators [MoA]
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2013-10-03
END MARKETING DATE: 0000-00-00


Duavee HUMAN PRESCRIPTION DRUG Details:

Item DescriptionDuavee from Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc.
LABELER NAME: Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: .45; 20(mg/1; mg/1)
START MARKETING DATE: 2013-10-03
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0008-1123_e61bb558-6bf7-4a6c-a4cd-bbb8f96e4e54
PRODUCT NDC: 0008-1123
APPLICATION NUMBER: NDA022247

Other ESTROGENS, CONJUGATED; BAZEDOXIFENE ACETATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
U.S. PharmaceuticalsDuavee
Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc.Duavee