GILDESS FE 1/20 (Par Pharmaceutical)
Welcome to the PulseAid listing for the GILDESS FE 1/20 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: | 2005-05-20 |
| END MARKETING DATE: | 2018-01-31 |
GILDESS FE 1/20 HUMAN PRESCRIPTION DRUG Details:
| Item Description | GILDESS FE 1/20 from Par Pharmaceutical |
| LABELER NAME: | Par Pharmaceutical |
| DEA SCHEDULE: | |
| ACTIVE STRENGTH: | () |
| START MARKETING DATE: | 2005-05-20 |
| END MARKETING DATE: | 2018-01-31 |
| PRODUCT ID: | 0603-7609_f6f597e6-f334-4f48-afd3-6165bc67cdfc |
| PRODUCT NDC: | 0603-7609 |
| APPLICATION NUMBER: | ANDA077077 |