Condylox (Actavis Pharma, Inc.)
Welcome to the PulseAid listing for the Condylox drug offered from Actavis Pharma, Inc.. This Decreased Mitosis [PE] 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: | podofilox |
SUBSTANCE NAME: | PODOFILOX |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Decreased Mitosis [PE] |
ROUTE: | TOPICAL |
DOSAGE FORM: | GEL |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 1997-03-13 |
END MARKETING DATE: | 0000-00-00 |
Condylox HUMAN PRESCRIPTION DRUG Details:
Item Description | Condylox from Actavis Pharma, Inc. |
LABELER NAME: | Actavis Pharma, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 5(mg/g) |
START MARKETING DATE: | 1997-03-13 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 52544-045_6352d35d-98cf-4674-9810-b9e485f25ef0 |
PRODUCT NDC: | 52544-045 |
APPLICATION NUMBER: | NDA020529 |
Other PODOFILOX Pharmaceutical Manufacturers / Labelers: