NDC 0008-1123
Duavee 20 mg / 0.45 mg tablet, film coated
On the label: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Pfizer Canada ULC | Brandon, Canada | Makes the active ingredient and tests it | No problems foundAug 3, 2023 · 4 inspections |
| Pfizer Ireland Pharmaceuticals Unlimited Company | Newbridge, Ireland | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilySep 23, 2022 · 8 inspections |
Product details
- Generic drug
- Bazedoxifene and Estrogens, Conjugated: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 20 mg / 0.45 mg
- Approval
- NDA NDA022247
- On the market since
- Oct 3, 2013
- Package NDCs
0008-1123-12- Official label
- DailyMed (National Library of Medicine), updated Apr 28, 2026
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