Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride (Sun Pharmaceutical Industries Limited)
Welcome to the PulseAid listing for the Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride drug offered from Sun Pharmaceutical Industries Limited. 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: | Sun Pharmaceutical Industries Limited |
NON-PROPRIETARY NAME: | Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride |
SUBSTANCE NAME: | CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, FILM COATED, EXTENDED RELEASE |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2012-09-29 |
END MARKETING DATE: | 0000-00-00 |
Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride HUMAN OTC DRUG Details:
Item Description | Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride from Sun Pharmaceutical Industries Limited |
LABELER NAME: | Sun Pharmaceutical Industries Limited |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 5; 120(mg/1; mg/1) |
START MARKETING DATE: | 2012-09-29 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 62756-915_873a7c4b-f995-44b8-8006-7b03b2eb1453 |
PRODUCT NDC: | 62756-915 |
APPLICATION NUMBER: | ANDA090922 |
Other CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: