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 |