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mercaptopurine - 68084-325-21 - (mercaptopurine)

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Drug Information of mercaptopurine

Product NDC: 68084-325
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: 68084-325
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040461
Marketing Category: ANDA
Start Marketing Date: 20130315

Package Information of mercaptopurine

Package NDC: 68084-325-21
Package Description: 3 BLISTER PACK in 1 CARTON (68084-325-21) > 10 TABLET in 1 BLISTER PACK (68084-325-01)

NDC Information of mercaptopurine

NDC Code 68084-325-21
Proprietary Name mercaptopurine
Package Description 3 BLISTER PACK in 1 CARTON (68084-325-21) > 10 TABLET in 1 BLISTER PACK (68084-325-01)
Product NDC 68084-325
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name mercaptopurine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130315
Marketing Category Name ANDA
Labeler Name American Health Packaging
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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