IMODIUMMulti-Symptom Relief (Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division)
Welcome to the PulseAid listing for the IMODIUM drug offered from Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division. This pharmaceutical is classified as a HUMAN OTC 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 OTC DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division |
| NON-PROPRIETARY NAME: | loperamide hydrochloride and dimethicone |
| SUBSTANCE NAME: | LOPERAMIDE HYDROCHLORIDE; DIMETHICONE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 2008-07-01 |
| END MARKETING DATE: | 0000-00-00 |
IMODIUM Multi-Symptom Relief HUMAN OTC DRUG Details:
| Item Description | IMODIUM Multi-Symptom Relief from Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division |
| LABELER NAME: | Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 2; 125(mg/1; mg/1) |
| START MARKETING DATE: | 2008-07-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 50580-338_bb6e86bb-fee4-45b1-ab6b-d9206998f362 |
| PRODUCT NDC: | 50580-338 |
| APPLICATION NUMBER: | NDA021140 |
Other LOPERAMIDE HYDROCHLORIDE; DIMETHICONE Pharmaceutical Manufacturers / Labelers:
