STAHIST AD (Magna Pharmaceuticals, Inc.)


Welcome to the PulseAid listing for the STAHIST AD drug offered from Magna 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: Magna Pharmaceuticals, Inc.
NON-PROPRIETARY NAME: CHLORCYCLIZINE HYDROCHLORIDE and PSEUDOEPHEDRINE HYDROCHLORIDE
SUBSTANCE NAME: CHLORCYCLIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2011-12-20
END MARKETING DATE: 0000-00-00


STAHIST AD HUMAN OTC DRUG Details:

Item DescriptionSTAHIST AD from Magna Pharmaceuticals, Inc.
LABELER NAME: Magna Pharmaceuticals, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 25; 60(mg/1; mg/1)
START MARKETING DATE: 2011-12-20
END MARKETING DATE: 0000-00-00
PRODUCT ID: 58407-625_cc22074a-f1c7-4e69-bfad-839de3f52505
PRODUCT NDC: 58407-625
APPLICATION NUMBER: part341

Other CHLORCYCLIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
MAGNA Pharmaceuticals, Inc.Stahist AD
Magna Pharmaceuticals, Inc.STAHIST AD