Glen PE (Glendale Inc)


Welcome to the PulseAid listing for the Glen PE 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: PHENYLEPHRINE HYDROCHLORIDE and PYRILAMINE MALEATE
SUBSTANCE NAME: PHENYLEPHRINE HYDROCHLORIDE; PYRILAMINE 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


Glen PE HUMAN OTC DRUG Details:

Item DescriptionGlen PE from Glendale Inc
LABELER NAME: Glendale Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 15; 16(mg/5mL; mg/5mL)
START MARKETING DATE: 2015-12-05
END MARKETING DATE: 0000-00-00
PRODUCT ID: 70147-224_00300957-6051-4c1f-b806-c62368dbe1f1
PRODUCT NDC: 70147-224
APPLICATION NUMBER: part341

Other PHENYLEPHRINE HYDROCHLORIDE; PYRILAMINE MALEATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Glendale IncGlen PE