Duavee is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Wyeth Pharmaceuticals Llc, A Subsidiary Of Pfizer Inc.. The primary component is Estrogens, Conjugated; Bazedoxifene Acetate.
Product ID | 0008-1123_221097d3-c86c-42b9-8ddd-ce7b4f89b6df |
NDC | 0008-1123 |
Product Type | Human Prescription Drug |
Proprietary Name | Duavee |
Generic Name | Conjugated Estrogens/bazedoxifene |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 2013-10-03 |
Marketing Category | NDA / NDA |
Application Number | NDA022247 |
Labeler Name | Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. |
Substance Name | ESTROGENS, CONJUGATED; BAZEDOXIFENE ACETATE |
Active Ingredient Strength | 0 mg/1; mg/1 |
Pharm Classes | Estrogen [EPC],Estrogen Receptor Agonists [MoA],Estrogens, Conjugated (USP) [CS],Estrogen Agonist/Antagonist [EPC],Selective Estrogen Receptor Modulators [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2013-10-03 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA022247 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-10-03 |
Ingredient | Strength |
---|---|
ESTROGENS, CONJUGATED | .45 mg/1 |
SPL SET ID: | e1b75458-2e5b-46b9-92c6-fa6daba3770f |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0008-1123 | Duavee | conjugated estrogens/bazedoxifene |
63539-112 | Duavee | conjugated estrogens/bazedoxifene |
63539-122 | Duavee | conjugated estrogens/bazedoxifene |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DUAVEE 86618211 4836834 Live/Registered |
Wyeth LLC 2015-05-04 |
DUAVEE 85840812 4544493 Live/Registered |
WYETH LLC 2013-02-05 |