Azurette is a Kit in the Human Prescription Drug category. It is labeled and distributed by Mayne Pharma Inc.. The primary component is .
Product ID | 51862-890_555bb0ac-47f9-4c8e-99e0-1c0e4b283b9a |
NDC | 51862-890 |
Product Type | Human Prescription Drug |
Proprietary Name | Azurette |
Generic Name | Desogestrel/ethinyl Estradiol And Ethinyl Estradiol |
Dosage Form | Kit |
Marketing Start Date | 2020-10-03 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA091247 |
Labeler Name | Mayne Pharma Inc. |
Active Ingredient Strength | 0 |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |
Marketing Start Date | 2020-10-03 |
NDC Exclude Flag | N |
Sample Package? | N |
NDC | Brand Name | Generic Name |
---|---|---|
51862-072 | Azurette | Desogestrel/Ethinyl Estradiol and Ethinyl Estradiol |
51862-890 | Azurette | desogestrel/ethinyl estradiol and ethinyl estradiol |
53002-1600 | Azurette | Desogestrel/Ethinyl Estradiol and Ethinyl Estradiol |
0555-9050 | Kariva | Desogestrel/Ethinyl Estradiol and Ethinyl Estradiol |
51285-120 | Mircette | Desogestrel/Ethinyl Estradiol and Ethinyl Estradiol |
16714-404 | PIMTREA | desogestrel/ethinyl estradiol and ethinyl estradiol |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
AZURETTE 78555788 3600154 Live/Registered |
MAYNE PHARMA LLC 2005-01-28 |