ZYRTEC-DAllergy and Congestion (Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division)
Welcome to the PulseAid listing for the ZYRTEC-D 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: | Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride |
| SUBSTANCE NAME: | CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, EXTENDED RELEASE |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 2008-01-01 |
| END MARKETING DATE: | 0000-00-00 |
ZYRTEC-D Allergy and Congestion HUMAN OTC DRUG Details:
| Item Description | ZYRTEC-D Allergy and Congestion 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: | 5; 120(mg/1; mg/1) |
| START MARKETING DATE: | 2008-01-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 50580-728_7d4dcae0-5c95-46ed-8dec-51a2d349ca26 |
| PRODUCT NDC: | 50580-728 |
| APPLICATION NUMBER: | NDA021150 |
Other CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
