Azurette is a Kit in the Human Prescription Drug category. It is labeled and distributed by Rpk Pharmaceuticals, Inc.. The primary component is .
| Product ID | 53002-1600_539ce389-ed65-4be7-9486-21518a2caf2c |
| NDC | 53002-1600 |
| 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 Category | ANDA / ANDA |
| Application Number | ANDA075863 |
| Labeler Name | RPK Pharmaceuticals, Inc. |
| Active Ingredient Strength | 0 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2017-09-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA075863 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2017-09-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA075863 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2017-09-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA075863 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2017-09-01 |
| Inactivation Date | 2020-01-31 |
| SPL SET ID: | 389c0c8b-b34d-47be-a45d-7ce2d6050382 |
| 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 |