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Allopurinol - 43063-079-30 - (allopurinol)

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Drug Information of Allopurinol

Product NDC: 43063-079
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: 43063-079
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075798
Marketing Category: ANDA
Start Marketing Date: 20030627

Package Information of Allopurinol

Package NDC: 43063-079-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (43063-079-30)

NDC Information of Allopurinol

NDC Code 43063-079-30
Proprietary Name Allopurinol
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (43063-079-30)
Product NDC 43063-079
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name allopurinol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030627
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, 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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