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: SOLUTION
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2010-05-17
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: 200; 10(mg/5mL; mg/5mL)
START MARKETING DATE: 2010-05-17
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0121-0809_58f894c7-263c-433a-af8d-7073c7079917
PRODUCT NDC: 0121-0809
APPLICATION NUMBER: part341

Other GUAIFENESIN; DEXTROMETHORPHAN Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Pharmaceutical Associates, Inc.GUAIFENESIN DM