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Allopurinol - 0591-5544-01 - (Allopurinol)

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Drug Information of Allopurinol

Product NDC: 0591-5544
Proprietary Name: Allopurinol
Non Proprietary Name: Allopurinol
Active Ingredient(s): 300    mg/1 & nbsp;   Allopurinol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Allopurinol

Product NDC: 0591-5544
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018877
Marketing Category: NDA
Start Marketing Date: 20090406

Package Information of Allopurinol

Package NDC: 0591-5544-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0591-5544-01)

NDC Information of Allopurinol

NDC Code 0591-5544-01
Proprietary Name Allopurinol
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0591-5544-01)
Product NDC 0591-5544
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Allopurinol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090406
Marketing Category Name NDA
Labeler Name Watson Laboratories, Inc.
Substance Name ALLOPURINOL
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]

Complete Information of Allopurinol


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