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Allopurinol - 54868-0075-4 - (Allopurinol)

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Drug Information of Allopurinol

Product NDC: 54868-0075
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: 54868-0075
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018832
Marketing Category: NDA
Start Marketing Date: 20020510

Package Information of Allopurinol

Package NDC: 54868-0075-4
Package Description: 100 TABLET in 1 BOTTLE (54868-0075-4)

NDC Information of Allopurinol

NDC Code 54868-0075-4
Proprietary Name Allopurinol
Package Description 100 TABLET in 1 BOTTLE (54868-0075-4)
Product NDC 54868-0075
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Allopurinol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020510
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name ALLOPURINOL
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]

Complete Information of Allopurinol


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