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Allopurinol - 52125-498-20 - (Allopurinol)

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Drug Information of Allopurinol

Product NDC: 52125-498
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: 52125-498
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090637
Marketing Category: ANDA
Start Marketing Date: 20130522

Package Information of Allopurinol

Package NDC: 52125-498-20
Package Description: 100 TABLET in 1 VIAL (52125-498-20)

NDC Information of Allopurinol

NDC Code 52125-498-20
Proprietary Name Allopurinol
Package Description 100 TABLET in 1 VIAL (52125-498-20)
Product NDC 52125-498
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Allopurinol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130522
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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