Layolis Fe (Actavis Pharma, Inc.)
Welcome to the PulseAid listing for the Layolis Fe drug offered from Actavis Pharma, 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: | Actavis Pharma, Inc. |
NON-PROPRIETARY NAME: | norethindrone, ethinyl estradiol, and ferrous fumarate |
SUBSTANCE NAME: | |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | KIT |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2011-12-23 |
END MARKETING DATE: | 0000-00-00 |
Layolis Fe HUMAN PRESCRIPTION DRUG Details:
Item Description | Layolis Fe from Actavis Pharma, Inc. |
LABELER NAME: | Actavis Pharma, Inc. |
DEA SCHEDULE: | |
ACTIVE STRENGTH: | () |
START MARKETING DATE: | 2011-12-23 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 52544-064_df48867f-93b4-4590-8ee3-cc01783c8860 |
PRODUCT NDC: | 52544-064 |
APPLICATION NUMBER: | NDA022573 |