Loratadine and Pseudoephedrine Sulfate (Sunmark)
Welcome to the PulseAid listing for the Loratadine and Pseudoephedrine Sulfate drug offered from Sunmark. 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: | Sunmark |
| NON-PROPRIETARY NAME: | Loratadine and Pseudoephedrine Sulfate |
| SUBSTANCE NAME: | LORATADINE; PSEUDOEPHEDRINE SULFATE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, FILM COATED, EXTENDED RELEASE |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2004-11-17 |
| END MARKETING DATE: | 0000-00-00 |
Loratadine and Pseudoephedrine Sulfate HUMAN OTC DRUG Details:
| Item Description | Loratadine and Pseudoephedrine Sulfate from Sunmark |
| LABELER NAME: | Sunmark |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 10; 240(mg/1; mg/1) |
| START MARKETING DATE: | 2004-11-17 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 49348-543_000c5c1b-d378-4acb-af47-5414dcab8b70 |
| PRODUCT NDC: | 49348-543 |
| APPLICATION NUMBER: | ANDA076557 |
Other LORATADINE; PSEUDOEPHEDRINE SULFATE Pharmaceutical Manufacturers / Labelers:
