VERMOX (Johnson & Johnson Consumer Inc, McNeil Consumer Healthcare Division)
Welcome to the PulseAid listing for the VERMOX drug offered from Johnson & Johnson Consumer Inc, McNeil Consumer Healthcare Division. This Antihelminthic [EPC] 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: | Johnson & Johnson Consumer Inc, McNeil Consumer Healthcare Division |
| NON-PROPRIETARY NAME: | mebendazole |
| SUBSTANCE NAME: | MEBENDAZOLE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Antihelminthic [EPC] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, CHEWABLE |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 1975-01-14 |
| END MARKETING DATE: | 0000-00-00 |
VERMOX HUMAN PRESCRIPTION DRUG Details:
| Item Description | VERMOX from Johnson & Johnson Consumer Inc, McNeil Consumer Healthcare Division |
| LABELER NAME: | Johnson & Johnson Consumer Inc, McNeil Consumer Healthcare Division |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 100(mg/1) |
| START MARKETING DATE: | 1975-01-14 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 50580-070_3e39b5e3-d0de-4d0d-93a5-071198551c0e |
| PRODUCT NDC: | 50580-070 |
| APPLICATION NUMBER: | NDA017481 |
Other MEBENDAZOLE Pharmaceutical Manufacturers / Labelers:
