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Allopurinol - 16714-042-06 - (Allopurinol)

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Drug Information of Allopurinol

Product NDC: 16714-042
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: 16714-042
Labeler Name: Northstar RxLLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078253
Marketing Category: ANDA
Start Marketing Date: 20091116

Package Information of Allopurinol

Package NDC: 16714-042-06
Package Description: 1000 TABLET in 1 BOTTLE (16714-042-06)

NDC Information of Allopurinol

NDC Code 16714-042-06
Proprietary Name Allopurinol
Package Description 1000 TABLET in 1 BOTTLE (16714-042-06)
Product NDC 16714-042
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Allopurinol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091116
Marketing Category Name ANDA
Labeler Name Northstar RxLLC
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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