Home > National Drug Code (NDC) > Allopurinol

Allopurinol - 0904-2614-61 - (Allopurinol)

Alphabetical Index


Drug Information of Allopurinol

Product NDC: 0904-2614
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: 0904-2614
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071450
Marketing Category: ANDA
Start Marketing Date: 20041210

Package Information of Allopurinol

Package NDC: 0904-2614-61
Package Description: 100 TABLET in 1 BOX, UNIT-DOSE (0904-2614-61)

NDC Information of Allopurinol

NDC Code 0904-2614-61
Proprietary Name Allopurinol
Package Description 100 TABLET in 1 BOX, UNIT-DOSE (0904-2614-61)
Product NDC 0904-2614
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Allopurinol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20041210
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name ALLOPURINOL
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]

Complete Information of Allopurinol


General Information