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Allopurinol - 62584-988-01 - (Allopurinol)

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Drug Information of Allopurinol

Product NDC: 62584-988
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: 62584-988
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA018832
Marketing Category: ANDA
Start Marketing Date: 20090311

Package Information of Allopurinol

Package NDC: 62584-988-01
Package Description: 10 BLISTER PACK in 1 CARTON (62584-988-01) > 10 TABLET in 1 BLISTER PACK (62584-988-11)

NDC Information of Allopurinol

NDC Code 62584-988-01
Proprietary Name Allopurinol
Package Description 10 BLISTER PACK in 1 CARTON (62584-988-01) > 10 TABLET in 1 BLISTER PACK (62584-988-11)
Product NDC 62584-988
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Allopurinol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090311
Marketing Category Name ANDA
Labeler Name American Health Packaging
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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