Panretin (Eisai Inc.)
Welcome to the PulseAid listing for the Panretin drug offered from Eisai Inc.. This Retinoid [EPC],Retinoids [Chemical/Ingredient] 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: | Eisai Inc. |
NON-PROPRIETARY NAME: | Alitretinoin |
SUBSTANCE NAME: | ALITRETINOIN |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Retinoid [EPC],Retinoids [Chemical/Ingredient] |
ROUTE: | TOPICAL |
DOSAGE FORM: | GEL |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2009-02-03 |
END MARKETING DATE: | 0000-00-00 |
Panretin HUMAN PRESCRIPTION DRUG Details:
Item Description | Panretin from Eisai Inc. |
LABELER NAME: | Eisai Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 60(mg/60g) |
START MARKETING DATE: | 2009-02-03 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 62856-601_1fa61b94-6ae2-4edc-85e0-8936108bda19 |
PRODUCT NDC: | 62856-601 |
APPLICATION NUMBER: | NDA020886 |
Other ALITRETINOIN Pharmaceutical Manufacturers / Labelers: