Allopurinol sodium (West-Ward Pharmaceuticals Corp)


Welcome to the PulseAid listing for the Allopurinol sodium drug offered from West-Ward Pharmaceuticals Corp. This Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION 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 PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: West-Ward Pharmaceuticals Corp
NON-PROPRIETARY NAME: Allopurinol sodium
SUBSTANCE NAME: ALLOPURINOL SODIUM
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2004-09-01
END MARKETING DATE: 0000-00-00


Allopurinol sodium HUMAN PRESCRIPTION DRUG Details:

Item DescriptionAllopurinol sodium from West-Ward Pharmaceuticals Corp
LABELER NAME: West-Ward Pharmaceuticals Corp
DEA SCHEDULE:
ACTIVE STRENGTH: 500(mg/25mL)
START MARKETING DATE: 2004-09-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0143-9533_5c4d416f-e181-4025-b89d-4edada3420b3
PRODUCT NDC: 0143-9533
APPLICATION NUMBER: ANDA076870

Other ALLOPURINOL SODIUM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
West-Ward Pharmaceuticals CorpAllopurinol sodium