Product NDC: | 65483-590 |
Proprietary Name: | IMURAN |
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) |
Product NDC: | 65483-590 |
Labeler Name: | Prometheus Laboratories Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA016324 |
Marketing Category: | NDA |
Start Marketing Date: | 19680320 |
Package NDC: | 65483-590-10 |
Package Description: | 100 TABLET in 1 BOTTLE (65483-590-10) |
NDC Code | 65483-590-10 |
Proprietary Name | IMURAN |
Package Description | 100 TABLET in 1 BOTTLE (65483-590-10) |
Product NDC | 65483-590 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | azathioprine |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19680320 |
Marketing Category Name | NDA |
Labeler Name | Prometheus Laboratories 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] |