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Allopurinol - 53808-0604-1 - (ALLOPURINOL)

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Drug Information of Allopurinol

Product NDC: 53808-0604
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: 53808-0604
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018832
Marketing Category: NDA
Start Marketing Date: 20090701

Package Information of Allopurinol

Package NDC: 53808-0604-1
Package Description: 30 TABLET in 1 BLISTER PACK (53808-0604-1)

NDC Information of Allopurinol

NDC Code 53808-0604-1
Proprietary Name Allopurinol
Package Description 30 TABLET in 1 BLISTER PACK (53808-0604-1)
Product NDC 53808-0604
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ALLOPURINOL
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name NDA
Labeler Name State of Florida DOH Central Pharmacy
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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