sunmark loratadine d (McKesson)
Welcome to the PulseAid listing for the sunmark loratadine d 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: | Loratadine, Pseudoephedrine |
| SUBSTANCE NAME: | LORATADINE; PSEUDOEPHEDRINE SULFATE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, EXTENDED RELEASE |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2012-03-06 |
| END MARKETING DATE: | 0000-00-00 |
sunmark loratadine d HUMAN OTC DRUG Details:
| Item Description | sunmark loratadine d from McKesson |
| LABELER NAME: | McKesson |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 5; 120(mg/1; mg/1) |
| START MARKETING DATE: | 2012-03-06 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 49348-183_ec0dc654-1569-4dbc-8dd0-ceacea213711 |
| PRODUCT NDC: | 49348-183 |
| APPLICATION NUMBER: | ANDA076050 |
Other LORATADINE; PSEUDOEPHEDRINE SULFATE Pharmaceutical Manufacturers / Labelers:
