Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride (Aurohealth LLC)
Welcome to the PulseAid listing for the Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride drug offered from Aurohealth LLC. 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: | Aurohealth LLC |
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: | 2017-10-30 |
END MARKETING DATE: | 0000-00-00 |
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride HUMAN OTC DRUG Details:
Item Description | Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride from Aurohealth LLC |
LABELER NAME: | Aurohealth LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 60; 120(mg/1; mg/1) |
START MARKETING DATE: | 2017-10-30 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 58602-807_4726af84-83c1-456d-995c-f6a8d1583f8b |
PRODUCT NDC: | 58602-807 |
APPLICATION NUMBER: | ANDA209116 |
Other FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: