| 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: | 0054-4581-11 |
| Package Description: | 25 TABLET in 1 BOTTLE, PLASTIC (0054-4581-11) |
| NDC Code | 0054-4581-11 |
| Proprietary Name | Mercaptopurine |
| Package Description | 25 TABLET in 1 BOTTLE, PLASTIC (0054-4581-11) |
| 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] |