Product NDC: | 49999-936 |
Proprietary Name: | CellCept |
Non Proprietary Name: | Mycophenolate Mofetil |
Active Ingredient(s): | 250 mg/1 & nbsp; Mycophenolate Mofetil |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49999-936 |
Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA050722 |
Marketing Category: | NDA |
Start Marketing Date: | 20111129 |
Package NDC: | 49999-936-00 |
Package Description: | 100 CAPSULE in 1 BOTTLE (49999-936-00) |
NDC Code | 49999-936-00 |
Proprietary Name | CellCept |
Package Description | 100 CAPSULE in 1 BOTTLE (49999-936-00) |
Product NDC | 49999-936 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Mycophenolate Mofetil |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20111129 |
Marketing Category Name | NDA |
Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Substance Name | MYCOPHENOLATE MOFETIL |
Strength Number | 250 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Antimetabolite Immunosuppressant [EPC] |