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Allopurinol - 68788-2115-1 - (Allopurinol)

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Drug Information of Allopurinol

Product NDC: 68788-2115
Proprietary Name: Allopurinol
Non Proprietary Name: Allopurinol
Active Ingredient(s): 100    mg/1 & nbsp;   Allopurinol
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Allopurinol

Product NDC: 68788-2115
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071586
Marketing Category: ANDA
Start Marketing Date: 20091001

Package Information of Allopurinol

Package NDC: 68788-2115-1
Package Description: 100 TABLET, COATED in 1 BOTTLE (68788-2115-1)

NDC Information of Allopurinol

NDC Code 68788-2115-1
Proprietary Name Allopurinol
Package Description 100 TABLET, COATED in 1 BOTTLE (68788-2115-1)
Product NDC 68788-2115
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Allopurinol
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20091001
Marketing Category Name ANDA
Labeler Name Preferred 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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