Lo Loestrin Fe (Allergan, Inc.)
Welcome to the PulseAid listing for the Lo Loestrin Fe drug offered from Allergan, 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: | Allergan, Inc. |
NON-PROPRIETARY NAME: | norethindrone acetate and ethinyl estradiol, ethinyl estradiol and ferrous fumarate |
SUBSTANCE NAME: | |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | |
DOSAGE FORM: | KIT |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2010-12-01 |
END MARKETING DATE: | 0000-00-00 |
Lo Loestrin Fe HUMAN PRESCRIPTION DRUG Details:
Item Description | Lo Loestrin Fe from Allergan, Inc. |
LABELER NAME: | Allergan, Inc. |
DEA SCHEDULE: | |
ACTIVE STRENGTH: | () |
START MARKETING DATE: | 2010-12-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0430-0420_97355bee-81c8-4f9a-8a33-67f798ae56f3 |
PRODUCT NDC: | 0430-0420 |
APPLICATION NUMBER: | NDA022501 |