SUNMARK 12 HOUR ALLERGY RELIEF (McKesson)
Welcome to the PulseAid listing for the SUNMARK 12 HOUR ALLERGY RELIEF drug offered from McKesson. 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: | McKesson |
| NON-PROPRIETARY NAME: | Clemastine fumarate |
| SUBSTANCE NAME: | CLEMASTINE FUMARATE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2003-07-03 |
| END MARKETING DATE: | 0000-00-00 |
SUNMARK 12 HOUR ALLERGY RELIEF HUMAN OTC DRUG Details:
| Item Description | SUNMARK 12 HOUR ALLERGY RELIEF from McKesson |
| LABELER NAME: | McKesson |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 1.34(mg/1) |
| START MARKETING DATE: | 2003-07-03 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 49348-686_539e2c02-b258-45ea-8694-58ce5165ea7c |
| PRODUCT NDC: | 49348-686 |
| APPLICATION NUMBER: | ANDA074512 |
Other CLEMASTINE FUMARATE Pharmaceutical Manufacturers / Labelers:
