Azasan - 65649-241-41 - (AZATHIOPRINE)

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Drug Information of Azasan

Product NDC: 65649-241
Proprietary Name: Azasan
Non Proprietary Name: AZATHIOPRINE
Active Ingredient(s): 100    mg/1 & nbsp;   AZATHIOPRINE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Azasan

Product NDC: 65649-241
Labeler Name: Salix Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075252
Marketing Category: ANDA
Start Marketing Date: 20030401

Package Information of Azasan

Package NDC: 65649-241-41
Package Description: 100 TABLET in 1 BOTTLE (65649-241-41)

NDC Information of Azasan

NDC Code 65649-241-41
Proprietary Name Azasan
Package Description 100 TABLET in 1 BOTTLE (65649-241-41)
Product NDC 65649-241
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name AZATHIOPRINE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030401
Marketing Category Name ANDA
Labeler Name Salix Pharmaceuticals, Inc.
Substance Name AZATHIOPRINE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Analog [Chemical/Ingredient],Purine Antimetabolite [EPC],Purines [Chemical/Ingredient]

Complete Information of Azasan


General Information