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Allopurinol - 53489-157-02 - (Allopurinol)

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Drug Information of Allopurinol

Product NDC: 53489-157
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: 53489-157
Labeler Name: Mutual Pharmaceutical
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071450
Marketing Category: ANDA
Start Marketing Date: 19870109

Package Information of Allopurinol

Package NDC: 53489-157-02
Package Description: 50 TABLET in 1 BOTTLE (53489-157-02)

NDC Information of Allopurinol

NDC Code 53489-157-02
Proprietary Name Allopurinol
Package Description 50 TABLET in 1 BOTTLE (53489-157-02)
Product NDC 53489-157
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Allopurinol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19870109
Marketing Category Name ANDA
Labeler Name Mutual Pharmaceutical
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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