GILDESS FE 1.5/30 (Par Pharmaceutical)
Welcome to the PulseAid listing for the GILDESS FE 1.5/30 drug offered from Par Pharmaceutical. 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: | Par Pharmaceutical |
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: | 2005-04-28 |
END MARKETING DATE: | 2018-01-31 |
GILDESS FE 1.5/30 HUMAN PRESCRIPTION DRUG Details:
Item Description | GILDESS FE 1.5/30 from Par Pharmaceutical |
LABELER NAME: | Par Pharmaceutical |
DEA SCHEDULE: | |
ACTIVE STRENGTH: | () |
START MARKETING DATE: | 2005-04-28 |
END MARKETING DATE: | 2018-01-31 |
PRODUCT ID: | 0603-7608_b051fef9-1691-464a-b6a1-623246e939f0 |
PRODUCT NDC: | 0603-7608 |
APPLICATION NUMBER: | ANDA077075 |