Zodryl DEC 40 (CodaDose, Inc.)


Welcome to the PulseAid listing for the Zodryl DEC 40 drug offered from CodaDose, 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: CodaDose, Inc.
NON-PROPRIETARY NAME: codeine phosphate, guaifenesin and pseudoephedrine hydrochloride
SUBSTANCE NAME: PSEUDOEPHEDRINE HYDROCHLORIDE; CODEINE PHOSPHATE; GUAIFENESIN
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: SUSPENSION
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2009-08-24
END MARKETING DATE: 0000-00-00


Zodryl DEC 40 HUMAN OTC DRUG Details:

Item DescriptionZodryl DEC 40 from CodaDose, Inc.
LABELER NAME: CodaDose, Inc.
DEA SCHEDULE: CV
ACTIVE STRENGTH: 14.998; 4.5; 90(mg/4.5mL; mg/4.5mL; mg/4.5mL)
START MARKETING DATE: 2009-08-24
END MARKETING DATE: 0000-00-00
PRODUCT ID: 43378-123_b51a9a1b-ddbe-47fc-bd22-d9e078dccb9b
PRODUCT NDC: 43378-123
APPLICATION NUMBER: part341

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

Manufacturer / LabelerProprietary Name
CodaDose, Inc.Zodryl DEC 25