Guaifenesin DAC (Rising Pharmaceuticals)


Welcome to the PulseAid listing for the Guaifenesin DAC drug offered from Rising Pharmaceuticals. 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: Rising Pharmaceuticals
NON-PROPRIETARY NAME: Guaifenesin, Codeine Phosphate and Pseudoephedrine Hydrochloride
SUBSTANCE NAME: GUAIFENESIN; CODEINE PHOSPHATE; PSEUDOEPHEDRINE HYDROCHLORIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2016-02-01
END MARKETING DATE: 0000-00-00


Guaifenesin DAC HUMAN OTC DRUG Details:

Item DescriptionGuaifenesin DAC from Rising Pharmaceuticals
LABELER NAME: Rising Pharmaceuticals
DEA SCHEDULE: CV
ACTIVE STRENGTH: 100; 10; 30(mg/5mL; mg/5mL; mg/5mL)
START MARKETING DATE: 2016-02-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 16571-301_da7c1b2a-b524-4661-a6c5-d355630d0ae8
PRODUCT NDC: 16571-301
APPLICATION NUMBER:

Other GUAIFENESIN; CODEINE PHOSPHATE; PSEUDOEPHEDRINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Rising PharmaceuticalsGuaifenesin DAC