M-ENDPE (R.A. McNeil Company)


Welcome to the PulseAid listing for the M-END drug offered from R.A. McNeil Company. 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: R.A. McNeil Company
NON-PROPRIETARY NAME: Codeine Phosphate, Phenylephrine Hydrochloride, Brompheniramine Maleate
SUBSTANCE NAME: CODEINE PHOSPHATE; PHENYLEPHRINE HYDROCHLORIDE; BROMPHENIRAMINE MALEATE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2008-11-11
END MARKETING DATE: 0000-00-00


M-END PE HUMAN OTC DRUG Details:

Item DescriptionM-END PE from R.A. McNeil Company
LABELER NAME: R.A. McNeil Company
DEA SCHEDULE: CV
ACTIVE STRENGTH: 6.33; 3.33; 1.33(mg/5mL; mg/5mL; mg/5mL)
START MARKETING DATE: 2008-11-11
END MARKETING DATE: 0000-00-00
PRODUCT ID: 12830-754_0b72a8c1-a03c-6522-e054-00144ff88e88
PRODUCT NDC: 12830-754
APPLICATION NUMBER: part341

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

Manufacturer / LabelerProprietary Name
R.A. McNeil CompanyM-END