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 Description | Guaifenesin 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: