Poly-Tussin AC (Poly Pharmaceuticals, Inc.)


Welcome to the PulseAid listing for the Poly-Tussin AC drug offered from Poly Pharmaceuticals, 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: Poly Pharmaceuticals, Inc.
NON-PROPRIETARY NAME: Brompheniramine Maleate, Codeine Phosphate, Phenylephrine Hydrochloride
SUBSTANCE NAME: BROMPHENIRAMINE MALEATE; CODEINE PHOSPHATE; PHENYLEPHRINE HYDROCHLORIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2014-06-02
END MARKETING DATE: 0000-00-00


Poly-Tussin AC HUMAN OTC DRUG Details:

Item DescriptionPoly-Tussin AC from Poly Pharmaceuticals, Inc.
LABELER NAME: Poly Pharmaceuticals, Inc.
DEA SCHEDULE: CV
ACTIVE STRENGTH: 4; 10; 10(mg/5mL; mg/5mL; mg/5mL)
START MARKETING DATE: 2014-06-02
END MARKETING DATE: 0000-00-00
PRODUCT ID: 50991-723_ca365aa2-9172-4ce7-8456-33c7fdf78d05
PRODUCT NDC: 50991-723
APPLICATION NUMBER: part341

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

Manufacturer / LabelerProprietary Name
Poly Pharmaceuticals, Inc.Poly-Tussin AC