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Azathioprine - 43353-686-60 - (Azathioprine)

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Drug Information of Azathioprine

Product NDC: 43353-686
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: 43353-686
Labeler Name: Aphena Pharma Solutions - Tennessee, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074069
Marketing Category: ANDA
Start Marketing Date: 19960216

Package Information of Azathioprine

Package NDC: 43353-686-60
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (43353-686-60)

NDC Information of Azathioprine

NDC Code 43353-686-60
Proprietary Name Azathioprine
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (43353-686-60)
Product NDC 43353-686
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Azathioprine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19960216
Marketing Category Name ANDA
Labeler Name Aphena Pharma Solutions - Tennessee, Inc.
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


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