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 |