Product NDC: | 0054-4581 |
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) |
Product NDC: | 0054-4581 |
Labeler Name: | Roxane Laboratories, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040528 |
Marketing Category: | ANDA |
Start Marketing Date: | 20040213 |
Package NDC: | 0054-4581-27 |
Package Description: | 250 TABLET in 1 BOTTLE, PLASTIC (0054-4581-27) |
NDC Code | 0054-4581-27 |
Proprietary Name | Mercaptopurine |
Package Description | 250 TABLET in 1 BOTTLE, PLASTIC (0054-4581-27) |
Product NDC | 0054-4581 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Mercaptopurine |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20040213 |
Marketing Category Name | ANDA |
Labeler Name | Roxane Laboratories, Inc |
Substance Name | MERCAPTOPURINE |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC] |