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Allopurinol - 51079-205-19 - (allopurinol)

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Drug Information of Allopurinol

Product NDC: 51079-205
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: 51079-205
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA018659
Marketing Category: ANDA
Start Marketing Date: 20130408

Package Information of Allopurinol

Package NDC: 51079-205-19
Package Description: 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-205-19) > 1 TABLET in 1 BLISTER PACK (51079-205-17)

NDC Information of Allopurinol

NDC Code 51079-205-19
Proprietary Name Allopurinol
Package Description 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-205-19) > 1 TABLET in 1 BLISTER PACK (51079-205-17)
Product NDC 51079-205
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name allopurinol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130408
Marketing Category Name ANDA
Labeler Name Mylan Institutional 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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