Product NDC: | 60951-735 |
Proprietary Name: | Mycophenolate Mofetil |
Non Proprietary Name: | mycophenolate mofetil |
Active Ingredient(s): | 500 mg/1 & nbsp; mycophenolate mofetil |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60951-735 |
Labeler Name: | Qualitest Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090606 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100719 |
Package NDC: | 60951-735-85 |
Package Description: | 500 TABLET in 1 BOTTLE (60951-735-85) |
NDC Code | 60951-735-85 |
Proprietary Name | Mycophenolate Mofetil |
Package Description | 500 TABLET in 1 BOTTLE (60951-735-85) |
Product NDC | 60951-735 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | mycophenolate mofetil |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20100719 |
Marketing Category Name | ANDA |
Labeler Name | Qualitest Pharmaceuticals |
Substance Name | MYCOPHENOLATE MOFETIL |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Antimetabolite Immunosuppressant [EPC] |