Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride (Sun Pharma Global FZE)
Welcome to the PulseAid listing for the Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride drug offered from Sun Pharma Global FZE. 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 Pharma Global FZE |
| NON-PROPRIETARY NAME: | Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride |
| SUBSTANCE NAME: | FEXOFENADINE 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: | 2015-02-13 |
| END MARKETING DATE: | 0000-00-00 |
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride HUMAN OTC DRUG Details:
| Item Description | Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride from Sun Pharma Global FZE |
| LABELER NAME: | Sun Pharma Global FZE |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 60; 120(mg/1; mg/1) |
| START MARKETING DATE: | 2015-02-13 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 47335-724_f23a4cbb-39b3-4c19-aeb4-11229c1c82bd |
| PRODUCT NDC: | 47335-724 |
| APPLICATION NUMBER: | ANDA090818 |
Other FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
