LOESTRIN Fe 1/2028 Day (Teva Women’s Health, Inc.)
Welcome to the PulseAid listing for the LOESTRIN Fe 1/20 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: | Norethindrone Acetate/Ethinyl Estradiol and Ferrous Fumarate |
SUBSTANCE NAME: | |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | |
DOSAGE FORM: | KIT |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2015-02-26 |
END MARKETING DATE: | 0000-00-00 |
LOESTRIN Fe 1/20 28 Day HUMAN PRESCRIPTION DRUG Details:
Item Description | LOESTRIN Fe 1/20 28 Day from Teva Women’s Health, Inc. |
LABELER NAME: | Teva Women’s Health, Inc. |
DEA SCHEDULE: | |
ACTIVE STRENGTH: | () |
START MARKETING DATE: | 2015-02-26 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 51285-125_d37e7e14-9f00-4805-a150-4d847ad7d559 |
PRODUCT NDC: | 51285-125 |
APPLICATION NUMBER: | ANDA076081 |