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: |
|
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: