Norel AD (US Pharmaceutical Corporation)


Welcome to the PulseAid listing for the Norel AD drug offered from US Pharmaceutical Corporation. This pharmaceutical is classified as a HUMAN OTC DRUG. Below, you can view the 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: US Pharmaceutical Corporation
NON-PROPRIETARY NAME: acetaminophen, chlorpheniramine maleate, and phenylephrine HCl
SUBSTANCE NAME: ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET, MULTILAYER
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2012-04-27
END MARKETING DATE: 0000-00-00


Norel AD HUMAN OTC DRUG Details:

Item DescriptionNorel AD from US Pharmaceutical Corporation
LABELER NAME: US Pharmaceutical Corporation
DEA SCHEDULE:
ACTIVE STRENGTH: 325; 4; 10(mg/1; mg/1; mg/1)
START MARKETING DATE: 2012-04-27
END MARKETING DATE: 0000-00-00
PRODUCT ID: 52747-475_5d801cfc-fd7e-fbeb-e053-2a91aa0aa33c
PRODUCT NDC: 52747-475
APPLICATION NUMBER: part341

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