Loratadine and Pseudoephedrine Sulfate (REMEDYREPACK INC.)
Welcome to the PulseAid listing for the Loratadine and Pseudoephedrine Sulfate drug offered from REMEDYREPACK INC.. 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: | REMEDYREPACK INC. |
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: | 2017-03-29 |
END MARKETING DATE: | 0000-00-00 |
Loratadine and Pseudoephedrine Sulfate HUMAN OTC DRUG Details:
Item Description | Loratadine and Pseudoephedrine Sulfate from REMEDYREPACK INC. |
LABELER NAME: | REMEDYREPACK INC. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 10; 240(mg/1; mg/1) |
START MARKETING DATE: | 2017-03-29 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 70518-0371_4d03bb2c-972f-533d-e054-00144ff8d46c |
PRODUCT NDC: | 70518-0371 |
APPLICATION NUMBER: | ANDA076557 |
Other LORATADINE; PSEUDOEPHEDRINE SULFATE Pharmaceutical Manufacturers / Labelers: