LORTUSSDM (Sallus Laboratories, LLC)


Welcome to the PulseAid listing for the LORTUSS drug offered from Sallus Laboratories, 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: Sallus Laboratories, LLC
NON-PROPRIETARY NAME: Dextromethorphan Hydrobromide, Doxylamine Succinate, Pseudoephedrine Hydrochloride
SUBSTANCE NAME: DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; PSEUDOEPHEDRINE HYDROCHLORIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2014-06-14
END MARKETING DATE: 0000-00-00


LORTUSS DM HUMAN OTC DRUG Details:

Item DescriptionLORTUSS DM from Sallus Laboratories, LLC
LABELER NAME: Sallus Laboratories, LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 15; 6.25; 30(mg/5mL; mg/5mL; mg/5mL)
START MARKETING DATE: 2014-06-14
END MARKETING DATE: 0000-00-00
PRODUCT ID: 69036-120_41999ae8-18fc-49a0-a55c-ffa00f353ddd
PRODUCT NDC: 69036-120
APPLICATION NUMBER: part341

Other DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; PSEUDOEPHEDRINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Sallus Laboratories, LLCLORTUSS