Product NDC: | 49999-937 |
Proprietary Name: | CellCept |
Non Proprietary Name: | Mycophenolate Mofetil |
Active Ingredient(s): | 500 mg/1 & nbsp; Mycophenolate Mofetil |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49999-937 |
Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA050723 |
Marketing Category: | NDA |
Start Marketing Date: | 19970619 |
Package NDC: | 49999-937-60 |
Package Description: | 60 TABLET, FILM COATED in 1 BOTTLE (49999-937-60) |
NDC Code | 49999-937-60 |
Proprietary Name | CellCept |
Package Description | 60 TABLET, FILM COATED in 1 BOTTLE (49999-937-60) |
Product NDC | 49999-937 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Mycophenolate Mofetil |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 19970619 |
Marketing Category Name | NDA |
Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Substance Name | MYCOPHENOLATE MOFETIL |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Antimetabolite Immunosuppressant [EPC] |