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Allopurinol - 49349-161-02 - (Allopurinol)

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Drug Information of Allopurinol

Product NDC: 49349-161
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: 49349-161
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090637
Marketing Category: ANDA
Start Marketing Date: 20110413

Package Information of Allopurinol

Package NDC: 49349-161-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-161-02)

NDC Information of Allopurinol

NDC Code 49349-161-02
Proprietary Name Allopurinol
Package Description 30 TABLET in 1 BLISTER PACK (49349-161-02)
Product NDC 49349-161
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Allopurinol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110413
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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