HISTEX-DM (Allegis Pharmaceuticals, LLC)


Welcome to the PulseAid listing for the HISTEX-DM drug offered from Allegis Pharmaceuticals, 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: Allegis Pharmaceuticals, LLC
NON-PROPRIETARY NAME: DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, and TRIPROLIDINE HYDROCHLORIDE
SUBSTANCE NAME: DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: SYRUP
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2014-03-19
END MARKETING DATE: 0000-00-00


HISTEX-DM HUMAN OTC DRUG Details:

Item DescriptionHISTEX-DM from Allegis Pharmaceuticals, LLC
LABELER NAME: Allegis Pharmaceuticals, LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 20; 10; 2.5(mg/5mL; mg/5mL; mg/5mL)
START MARKETING DATE: 2014-03-19
END MARKETING DATE: 0000-00-00
PRODUCT ID: 28595-804_ac2157ef-390a-4c6d-a304-9e78aae1294d
PRODUCT NDC: 28595-804
APPLICATION NUMBER: part341

Other DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Allegis Pharmaceuticals, LLCHISTEX-DM