Desloratadine (Sun Pharmaceutical Industries Limited)
Welcome to the PulseAid listing for the Desloratadine drug offered from Sun Pharmaceutical Industries Limited. This Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] pharmaceutical is classified as a HUMAN PRESCRIPTION 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 PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: | Sun Pharmaceutical Industries Limited |
NON-PROPRIETARY NAME: | Desloratadine |
SUBSTANCE NAME: | DESLORATADINE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, FILM COATED |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2010-11-24 |
END MARKETING DATE: | 0000-00-00 |
Desloratadine HUMAN PRESCRIPTION DRUG Details:
Item Description | Desloratadine from Sun Pharmaceutical Industries Limited |
LABELER NAME: | Sun Pharmaceutical Industries Limited |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 5(mg/1) |
START MARKETING DATE: | 2010-11-24 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 62756-523_92946a6c-8da6-42cf-b407-1cd12c4199ba |
PRODUCT NDC: | 62756-523 |
APPLICATION NUMBER: | ANDA078359 |
Other DESLORATADINE Pharmaceutical Manufacturers / Labelers: