Azurette (Watson Pharma, Inc.)
Welcome to the PulseAid listing for the Azurette drug offered from Watson Pharma, Inc.. This pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: | Watson Pharma, Inc. |
NON-PROPRIETARY NAME: | Desogestrel/Ethinyl Estradiol and Ethinyl Estradiol |
SUBSTANCE NAME: | |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | |
DOSAGE FORM: | KIT |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2008-12-29 |
END MARKETING DATE: | 0000-00-00 |
Azurette HUMAN PRESCRIPTION DRUG Details:
Item Description | Azurette from Watson Pharma, Inc. |
LABELER NAME: | Watson Pharma, Inc. |
DEA SCHEDULE: | |
ACTIVE STRENGTH: | () |
START MARKETING DATE: | 2008-12-29 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 52544-940_e53e6005-b8ce-44f1-ba32-f2691b4d59c0 |
PRODUCT NDC: | 52544-940 |
APPLICATION NUMBER: | ANDA076916 |