ZYLOPRIM - 65483-993-10 - (allopurinol)

Alphabetical Index


Drug Information of ZYLOPRIM

Product NDC: 65483-993
Proprietary Name: ZYLOPRIM
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 ZYLOPRIM

Product NDC: 65483-993
Labeler Name: Prometheus Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA016084
Marketing Category: NDA
Start Marketing Date: 19660819

Package Information of ZYLOPRIM

Package NDC: 65483-993-10
Package Description: 100 TABLET in 1 BOTTLE (65483-993-10)

NDC Information of ZYLOPRIM

NDC Code 65483-993-10
Proprietary Name ZYLOPRIM
Package Description 100 TABLET in 1 BOTTLE (65483-993-10)
Product NDC 65483-993
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name allopurinol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19660819
Marketing Category Name NDA
Labeler Name Prometheus Laboratories Inc.
Substance Name ALLOPURINOL
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]

Complete Information of ZYLOPRIM


General Information