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Azathioprine - 54868-5310-0 - (Azathioprine)

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Drug Information of Azathioprine

Product NDC: 54868-5310
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: 54868-5310
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077621
Marketing Category: ANDA
Start Marketing Date: 20050523

Package Information of Azathioprine

Package NDC: 54868-5310-0
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (54868-5310-0)

NDC Information of Azathioprine

NDC Code 54868-5310-0
Proprietary Name Azathioprine
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (54868-5310-0)
Product NDC 54868-5310
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Azathioprine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050523
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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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