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Azathioprine - 68462-502-01 - (Azathioprine)

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Drug Information of Azathioprine

Product NDC: 68462-502
Proprietary Name: Azathioprine
Non Proprietary Name: Azathioprine
Active Ingredient(s): 50    mg/1 & nbsp;   Azathioprine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Azathioprine

Product NDC: 68462-502
Labeler Name: Glenmark Generics Inc., USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075252
Marketing Category: ANDA
Start Marketing Date: 20081120

Package Information of Azathioprine

Package NDC: 68462-502-01
Package Description: 100 TABLET in 1 BOTTLE (68462-502-01)

NDC Information of Azathioprine

NDC Code 68462-502-01
Proprietary Name Azathioprine
Package Description 100 TABLET in 1 BOTTLE (68462-502-01)
Product NDC 68462-502
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Azathioprine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20081120
Marketing Category Name ANDA
Labeler Name Glenmark Generics Inc., USA
Substance Name AZATHIOPRINE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Analog [Chemical/Ingredient],Purine Antimetabolite [EPC],Purines [Chemical/Ingredient]

Complete Information of Azathioprine


General Information