MENTAX (Mylan Pharmaceuticals Inc.)
Welcome to the PulseAid listing for the MENTAX drug offered from Mylan Pharmaceuticals Inc.. This Benzylamine Antifungal [EPC],Benzylamines [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: | Mylan Pharmaceuticals Inc. |
NON-PROPRIETARY NAME: | butenafine hydrochloride |
SUBSTANCE NAME: | BUTENAFINE HYDROCHLORIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Benzylamine Antifungal [EPC],Benzylamines [Chemical/Ingredient] |
ROUTE: | TOPICAL |
DOSAGE FORM: | CREAM |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 1996-12-31 |
END MARKETING DATE: | 0000-00-00 |
MENTAX HUMAN PRESCRIPTION DRUG Details:
Item Description | MENTAX from Mylan Pharmaceuticals Inc. |
LABELER NAME: | Mylan Pharmaceuticals Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 10(mg/g) |
START MARKETING DATE: | 1996-12-31 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0378-6151_b856f519-0749-4f1d-9846-a90ff5ad0e5f |
PRODUCT NDC: | 0378-6151 |
APPLICATION NUMBER: | NDA020524 |
Other BUTENAFINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: