Duraflu (Poly Pharmaceuticals, Inc.)


Welcome to the PulseAid listing for the Duraflu drug offered from Poly 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: Poly Pharmaceuticals, Inc.
NON-PROPRIETARY NAME: ACETAMINOPHEN, DEXTROMETHORPHAN HBr, GUAIFENESIN, PSEUDOEPHEDRINE HCl
SUBSTANCE NAME: ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2015-10-01
END MARKETING DATE: 0000-00-00


Duraflu HUMAN OTC DRUG Details:

Item DescriptionDuraflu from Poly Pharmaceuticals, Inc.
LABELER NAME: Poly Pharmaceuticals, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 325; 20; 200; 60(mg/1; mg/1; mg/1; mg/1)
START MARKETING DATE: 2015-10-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 50991-535_3f767a59-37fc-4646-ab6b-d571b1f0962c
PRODUCT NDC: 50991-535
APPLICATION NUMBER: part341

Other ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Poly Pharmaceuticals, Inc.Duraflu