GUAIFENESIN DM (Pharmaceutical Associates, Inc.)


Welcome to the PulseAid listing for the GUAIFENESIN DM drug offered from Pharmaceutical Associates, 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: Pharmaceutical Associates, Inc.
NON-PROPRIETARY NAME: GUAIFENESIN and DEXTROMETHORPHAN
SUBSTANCE NAME: GUAIFENESIN; DEXTROMETHORPHAN
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: SYRUP
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 1992-07-01
END MARKETING DATE: 0000-00-00


GUAIFENESIN DM HUMAN OTC DRUG Details:

Item DescriptionGUAIFENESIN DM from Pharmaceutical Associates, Inc.
LABELER NAME: Pharmaceutical Associates, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 100; 10(mg/5mL; mg/5mL)
START MARKETING DATE: 1992-07-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0121-0638_4b481e49-7547-3345-e054-00144ff8d46c
PRODUCT NDC: 0121-0638
APPLICATION NUMBER: part341

Other GUAIFENESIN; DEXTROMETHORPHAN Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Pharmaceutical Associates, Inc.GUAIFENESIN DM