Home > National Drug Code (NDC) > Allopurinol

Allopurinol - 24236-214-20 - (Allopurinol)

Alphabetical Index


Drug Information of Allopurinol

Product NDC: 24236-214
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: 24236-214
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018832
Marketing Category: NDA
Start Marketing Date: 20130213

Package Information of Allopurinol

Package NDC: 24236-214-20
Package Description: 100 TABLET in 1 VIAL (24236-214-20)

NDC Information of Allopurinol

NDC Code 24236-214-20
Proprietary Name Allopurinol
Package Description 100 TABLET in 1 VIAL (24236-214-20)
Product NDC 24236-214
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Allopurinol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130213
Marketing Category Name NDA
Labeler Name REMEDYREPACK 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


General Information