Junel Fe 1/20 (Preferred Pharmaceuticals Inc.)
Welcome to the PulseAid listing for the Junel Fe 1/20 drug offered from Preferred Pharmaceuticals 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: | Preferred Pharmaceuticals Inc. |
| NON-PROPRIETARY NAME: | norethindrone acetate and ethinyl estradiol, and ferrous fumarate |
| SUBSTANCE NAME: | |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | |
| DOSAGE FORM: | KIT |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2016-11-21 |
| END MARKETING DATE: | 0000-00-00 |
Junel Fe 1/20 HUMAN PRESCRIPTION DRUG Details:
| Item Description | Junel Fe 1/20 from Preferred Pharmaceuticals Inc. |
| LABELER NAME: | Preferred Pharmaceuticals Inc. |
| DEA SCHEDULE: | |
| ACTIVE STRENGTH: | () |
| START MARKETING DATE: | 2016-11-21 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 68788-6832_a76090ab-a8b3-497f-a72d-2bf40fba37d6 |
| PRODUCT NDC: | 68788-6832 |
| APPLICATION NUMBER: | ANDA076081 |