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mercaptopurine - 49884-922-04 - (mercaptopurine)

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Drug Information of mercaptopurine

Product NDC: 49884-922
Proprietary Name: mercaptopurine
Non Proprietary Name: mercaptopurine
Active Ingredient(s): 50    mg/1 & nbsp;   mercaptopurine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of mercaptopurine

Product NDC: 49884-922
Labeler Name: Par Pharmaceutical Companies, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040461
Marketing Category: ANDA
Start Marketing Date: 20040211

Package Information of mercaptopurine

Package NDC: 49884-922-04
Package Description: 250 TABLET in 1 BOTTLE (49884-922-04)

NDC Information of mercaptopurine

NDC Code 49884-922-04
Proprietary Name mercaptopurine
Package Description 250 TABLET in 1 BOTTLE (49884-922-04)
Product NDC 49884-922
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name mercaptopurine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040211
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical Companies, Inc.
Substance Name MERCAPTOPURINE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC]

Complete Information of mercaptopurine


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