Azurette
desogestrel/ethinyl estradiol and ethinyl estradiol · KIT · Dr. Reddys Laboratories Inc.
No Recall History
Plain English
Azurette is a kit containing desogestrel/ethinyl estradiol and ethinyl estradiol. Manufactured by Dr. Reddys Laboratories Inc..
Key Facts
- Brand Name
- Azurette
- Generic Name
- desogestrel/ethinyl estradiol and ethinyl estradiol
- NDC Code (Product)
75907-091- Manufacturer
- Dr. Reddys Laboratories Inc.
- Dosage Form
- KIT
- Marketing Status
- Application #
- ANDA091247
- Marketing Start
- 06/25/2024
Recall History
No Recall HistoryFrequently 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 75907-091, listed by Dr. Reddys Laboratories Inc..