Duavee 20 mg/1
conjugated estrogens/bazedoxifene · TABLET, FILM COATED · Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
Duavee is a tablet, film coated containing conjugated estrogens/bazedoxifene at 20 mg/1, taken oral. Manufactured by Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc..
Key Facts
- Brand Name
- Duavee
- Generic Name
- conjugated estrogens/bazedoxifene
- NDC Code (Product)
0008-1123- Manufacturer
- Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
- Strength
- 20 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- NDA022247
- Drug Class
- Estrogen [EPC]
- Marketing Start
- 10/03/2013
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
Frequently Asked Questions
What is Duavee used for?
Duavee contains conjugated estrogens/bazedoxifene. It is a tablet, film coated taken oral. Consult your doctor for specific uses.
Is Duavee a controlled substance?
Duavee is not classified as a controlled substance by the DEA.
What is the generic name for Duavee?
The generic name for Duavee is conjugated estrogens/bazedoxifene. There are no other listed brand versions of conjugated estrogens/bazedoxifene.
What is the NDC code for Duavee 20 mg/1?
The NDC (National Drug Code) for Duavee 20 mg/1 is 0008-1123, listed by Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc..
Other Duavee Dosages
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)