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Allopurinol - 55154-6222-9 - (Allopurinol)

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Drug Information of Allopurinol

Product NDC: 55154-6222
Proprietary Name: Allopurinol
Non Proprietary Name: Allopurinol
Active Ingredient(s): 100    mg/1 & nbsp;   Allopurinol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Allopurinol

Product NDC: 55154-6222
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018659
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19861024

Package Information of Allopurinol

Package NDC: 55154-6222-9
Package Description: 6 BLISTER PACK in 1 CARTON (55154-6222-9) > 5 TABLET in 1 BLISTER PACK

NDC Information of Allopurinol

NDC Code 55154-6222-9
Proprietary Name Allopurinol
Package Description 6 BLISTER PACK in 1 CARTON (55154-6222-9) > 5 TABLET in 1 BLISTER PACK
Product NDC 55154-6222
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Allopurinol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19861024
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Cardinal Health
Substance Name ALLOPURINOL
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]

Complete Information of Allopurinol


General Information