M-ENDDMX (R. A. McNeil Company)


Welcome to the PulseAid listing for the M-END drug offered from R. A. McNeil Company. 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: R. A. McNeil Company
NON-PROPRIETARY NAME: Dexbrompheniramine Maleate, Dextromethorphan Hydrobromide, Pseudoephedrine Hydrochloride
SUBSTANCE NAME: DEXBROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2011-10-13
END MARKETING DATE: 0000-00-00


M-END DMX HUMAN OTC DRUG Details:

Item DescriptionM-END DMX from R. A. McNeil Company
LABELER NAME: R. A. McNeil Company
DEA SCHEDULE:
ACTIVE STRENGTH: .667; 10; 20(mg/5mL; mg/5mL; mg/5mL)
START MARKETING DATE: 2011-10-13
END MARKETING DATE: 0000-00-00
PRODUCT ID: 12830-816_47a8c346-578e-05b1-e054-00144ff88e88
PRODUCT NDC: 12830-816
APPLICATION NUMBER: part341

Other DEXBROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PSEUDOEPHEDRINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
R. A. McNeil CompanyM-END