Drugplain

Azurette

desogestrel/ethinyl estradiol and ethinyl estradiol · KIT · Mayne Pharma Inc.

No Recall History
Plain English

Azurette is a kit containing desogestrel/ethinyl estradiol and ethinyl estradiol. Manufactured by Mayne Pharma Inc..

Key Facts

Brand Name
Azurette
Generic Name
desogestrel/ethinyl estradiol and ethinyl estradiol
NDC Code (Product)
51862-890
Manufacturer
Mayne Pharma Inc.
Dosage Form
KIT
Marketing Status
Application #
ANDA091247
Marketing Start
10/03/2020

Recall History

No Recall History

Frequently Asked Questions

What is Azurette used for?

Azurette contains desogestrel/ethinyl estradiol and ethinyl estradiol. It is a kit taken as directed. Consult your doctor for specific uses.

Is Azurette a controlled substance?

Azurette is not classified as a controlled substance by the DEA.

What is the generic name for Azurette?

The generic name for Azurette is desogestrel/ethinyl estradiol and ethinyl estradiol. There are 2 other brand versions of desogestrel/ethinyl estradiol and ethinyl estradiol.

What is the NDC code for Azurette ?

The NDC (National Drug Code) for Azurette is 51862-890, listed by Mayne Pharma Inc..

Product NDC

51862-890

Package NDC

51862-890-01

Other Azurette Dosages

Other Desogestrel/ethinyl Brands

See all →

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)