Acthrel (Ferring Pharmaceuticals Inc.)
Welcome to the PulseAid listing for the Acthrel drug offered from Ferring 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: | Ferring Pharmaceuticals Inc. |
| NON-PROPRIETARY NAME: | Corticorelin ovine triflutate |
| SUBSTANCE NAME: | CORTICORELIN OVINE TRIFLUTATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 1996-05-23 |
| END MARKETING DATE: | 0000-00-00 |
Acthrel HUMAN PRESCRIPTION DRUG Details:
| Item Description | Acthrel from Ferring Pharmaceuticals Inc. |
| LABELER NAME: | Ferring Pharmaceuticals Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 100(ug/2mL) |
| START MARKETING DATE: | 1996-05-23 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 55566-0302_4698848e-3251-49f8-bcac-614fd485c784 |
| PRODUCT NDC: | 55566-0302 |
| APPLICATION NUMBER: | NDA020162 |
Other CORTICORELIN OVINE TRIFLUTATE Pharmaceutical Manufacturers / Labelers:
