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ALLOPURINOL - 42549-500-60 - (ALLOPURINOL)

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Drug Information of ALLOPURINOL

Product NDC: 42549-500
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: 42549-500
Labeler Name: STAT Rx USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075798
Marketing Category: ANDA
Start Marketing Date: 20030627

Package Information of ALLOPURINOL

Package NDC: 42549-500-60
Package Description: 60 TABLET in 1 BOTTLE (42549-500-60)

NDC Information of ALLOPURINOL

NDC Code 42549-500-60
Proprietary Name ALLOPURINOL
Package Description 60 TABLET in 1 BOTTLE (42549-500-60)
Product NDC 42549-500
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ALLOPURINOL
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030627
Marketing Category Name ANDA
Labeler Name STAT Rx USA LLC
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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