Glenmax PEB DM FORTE (Glendale Inc)


Welcome to the PulseAid listing for the Glenmax PEB DM FORTE 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 FORTE HUMAN OTC DRUG Details:

Item DescriptionGlenmax PEB DM FORTE from Glendale Inc
LABELER NAME: Glendale Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 20; 10; 4(mg/5mL; mg/5mL; mg/5mL)
START MARKETING DATE: 2015-12-05
END MARKETING DATE: 0000-00-00
PRODUCT ID: 70147-223_a072f9ee-7b72-4c8f-81db-9f0b2e022a67
PRODUCT NDC: 70147-223
APPLICATION NUMBER: part341

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

Manufacturer / LabelerProprietary Name
Glendale IncGlenmax PEB DM FORTE