QUARTETTE (Teva Women’s Health, Inc.)
Welcome to the PulseAid listing for the QUARTETTE drug offered from Teva Women’s Health, 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: | Teva Women’s Health, Inc. |
NON-PROPRIETARY NAME: | Levonorgestrel/Ethinyl Estradiol and Ethinyl Estradiol |
SUBSTANCE NAME: | |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | |
DOSAGE FORM: | KIT |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2013-07-25 |
END MARKETING DATE: | 0000-00-00 |
QUARTETTE HUMAN PRESCRIPTION DRUG Details:
Item Description | QUARTETTE from Teva Women’s Health, Inc. |
LABELER NAME: | Teva Women’s Health, Inc. |
DEA SCHEDULE: | |
ACTIVE STRENGTH: | () |
START MARKETING DATE: | 2013-07-25 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 51285-431_ee49aaee-e443-43b0-ad5e-3afd5e02a3d2 |
PRODUCT NDC: | 51285-431 |
APPLICATION NUMBER: | NDA204061 |