PRO-REDAC (Pro-Pharma, LLC)


Welcome to the PulseAid listing for the PRO-RED drug offered from Pro-Pharma, LLC. 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: Pro-Pharma, LLC
NON-PROPRIETARY NAME: Codeine Phosphate, Dexchorpheniramine Maleate, Phenylephrine Hydrochloride
SUBSTANCE NAME: CODEINE PHOSPHATE; DEXCHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: SYRUP
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2013-09-30
END MARKETING DATE: 0000-00-00


PRO-RED AC HUMAN OTC DRUG Details:

Item DescriptionPRO-RED AC from Pro-Pharma, LLC
LABELER NAME: Pro-Pharma, LLC
DEA SCHEDULE: CV
ACTIVE STRENGTH: 9; 1; 5(mg/5mL; mg/5mL; mg/5mL)
START MARKETING DATE: 2013-09-30
END MARKETING DATE: 0000-00-00
PRODUCT ID: 66594-499_cc958709-6208-4ae0-8d57-2361bf78d826
PRODUCT NDC: 66594-499
APPLICATION NUMBER: part341

Other CODEINE PHOSPHATE; DEXCHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Pro-Pharma, LLCPRO-RED