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 | 51862-072_2bdaa40c-cf4b-4413-bb80-b1b6c5bcc352 |
| NDC | 51862-072 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Azurette |
| Generic Name | Desogestrel/ethinyl Estradiol And Ethinyl Estradiol |
| Dosage Form | Kit |
| Marketing Start Date | 2016-11-14 |
| Marketing End Date | 2022-03-31 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA075863 |
| Labeler Name | Mayne Pharma Inc. |
| Active Ingredient Strength | 0 |
| NDC Exclude Flag | N |
| Marketing Start Date | 2016-11-14 |
| Marketing End Date | 2022-03-31 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA075863 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2016-11-14 |
| Marketing Category | ANDA |
| Application Number | ANDA075863 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2016-11-14 |
| SPL SET ID: | ce13d459-3096-4899-9975-7e932260a14f |
| Manufacturer | |
| RxNorm Concept Unique ID - RxCUI |
| 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 |