Glentuss (Glendale Inc)
Welcome to the PulseAid listing for the Glentuss drug offered from Glendale Inc. 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: | Glendale Inc |
NON-PROPRIETARY NAME: | DEXTROMETHORPHAN HYDROBROMIDE, PSEUDOEPHEDRINE HYDROCHLORIDE, and DOXYLAMINE SUCCINATE |
SUBSTANCE NAME: | DEXTROMETHORPHAN HYDROBROMIDE; PSEUDOEPHEDRINE HYDROCHLORIDE; DOXYLAMINE SUCCINATE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | SYRUP |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2015-12-05 |
END MARKETING DATE: | 0000-00-00 |
Glentuss HUMAN OTC DRUG Details:
Item Description | Glentuss from Glendale Inc |
LABELER NAME: | Glendale Inc |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 15; 30; 6.25(mg/5mL; mg/5mL; mg/5mL) |
START MARKETING DATE: | 2015-12-05 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 70147-233_f23182eb-a618-4556-a265-3de318cc7ae5 |
PRODUCT NDC: | 70147-233 |
APPLICATION NUMBER: | part341 |
Other DEXTROMETHORPHAN HYDROBROMIDE; PSEUDOEPHEDRINE HYDROCHLORIDE; DOXYLAMINE SUCCINATE Pharmaceutical Manufacturers / Labelers: