NorelCSCS (US Pharmaceutical Corporation)
Welcome to the PulseAid listing for the NorelCS drug offered from US Pharmaceutical Corporation. 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: | US Pharmaceutical Corporation |
NON-PROPRIETARY NAME: | Chlorpheniramine Maleate/Dextromethorphan Hydrobromide/Phenylephrine Hydrochloride |
SUBSTANCE NAME: | CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | LIQUID |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2012-08-01 |
END MARKETING DATE: | 0000-00-00 |
NorelCS CS HUMAN OTC DRUG Details:
Item Description | NorelCS CS from US Pharmaceutical Corporation |
LABELER NAME: | US Pharmaceutical Corporation |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 4; 12.5; 10(mg/5mL; mg/5mL; mg/5mL) |
START MARKETING DATE: | 2012-08-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 52747-480_51fa1666-3a2d-401c-afc2-85641bd92258 |
PRODUCT NDC: | 52747-480 |
APPLICATION NUMBER: | part341 |
Other CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: