ED BRON GP (EDWARDS PHARMACEUTICALS, INC.)


Welcome to the PulseAid listing for the ED BRON GP drug offered from EDWARDS PHARMACEUTICALS, 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: EDWARDS PHARMACEUTICALS, INC.
NON-PROPRIETARY NAME: GUAIFENESIN and PHENYLEPHRINE
SUBSTANCE NAME: GUAIFENESIN; PHENYLEPHRINE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2012-06-01
END MARKETING DATE: 0000-00-00


ED BRON GP HUMAN OTC DRUG Details:

Item DescriptionED BRON GP from EDWARDS PHARMACEUTICALS, INC.
LABELER NAME: EDWARDS PHARMACEUTICALS, INC.
DEA SCHEDULE:
ACTIVE STRENGTH: 100; 5(mg/5mL; mg/5mL)
START MARKETING DATE: 2012-06-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0485-0208_fea45bff-6e84-492c-b9f0-eae03248536f
PRODUCT NDC: 0485-0208
APPLICATION NUMBER: part341

Other GUAIFENESIN; PHENYLEPHRINE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
EDWARDS PHARMACEUTICALS, INC.ED BRON GP