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Allopurinol - 0615-1592-39 - (Allopurinol)

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Drug Information of Allopurinol

Product NDC: 0615-1592
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: 0615-1592
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018659
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19861024

Package Information of Allopurinol

Package NDC: 0615-1592-39
Package Description: 30 TABLET in 1 BLISTER PACK (0615-1592-39)

NDC Information of Allopurinol

NDC Code 0615-1592-39
Proprietary Name Allopurinol
Package Description 30 TABLET in 1 BLISTER PACK (0615-1592-39)
Product NDC 0615-1592
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Allopurinol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19861024
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name ALLOPURINOL
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]

Complete Information of Allopurinol


General Information