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Allopurinol - 52125-128-02 - (ALLOPURINOL)

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Drug Information of Allopurinol

Product NDC: 52125-128
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: 52125-128
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075798
Marketing Category: ANDA
Start Marketing Date: 20120928

Package Information of Allopurinol

Package NDC: 52125-128-02
Package Description: 30 TABLET in 1 BLISTER PACK (52125-128-02)

NDC Information of Allopurinol

NDC Code 52125-128-02
Proprietary Name Allopurinol
Package Description 30 TABLET in 1 BLISTER PACK (52125-128-02)
Product NDC 52125-128
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ALLOPURINOL
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120928
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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