Glenmax PEB DM (Glendale Inc)


Welcome to the PulseAid listing for the Glenmax PEB DM 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, PHENYLEPHRINE HYDROCHLORIDE, and BROMPHENIRAMINE MALEATE
SUBSTANCE NAME: DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; BROMPHENIRAMINE MALEATE
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


Glenmax PEB DM HUMAN OTC DRUG Details:

Item DescriptionGlenmax PEB DM from Glendale Inc
LABELER NAME: Glendale Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 10; 5; 2(mg/5mL; mg/5mL; mg/5mL)
START MARKETING DATE: 2015-12-05
END MARKETING DATE: 0000-00-00
PRODUCT ID: 70147-230_7fe86587-1b8a-46c4-bb15-0882d3cf141c
PRODUCT NDC: 70147-230
APPLICATION NUMBER: part341

Other DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; BROMPHENIRAMINE MALEATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Glendale IncGlenmax PEB DM FORTE