CellCept is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Genentech, Inc.. The primary component is Mycophenolate Mofetil.
| Product ID | 0004-0260_069ac782-5550-41a9-9179-bc1e44430526 |
| NDC | 0004-0260 |
| Product Type | Human Prescription Drug |
| Proprietary Name | CellCept |
| Generic Name | Mycophenolate Mofetil |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 1997-06-19 |
| Marketing Category | NDA / NDA |
| Application Number | NDA050723 |
| Labeler Name | Genentech, Inc. |
| Substance Name | MYCOPHENOLATE MOFETIL |
| Active Ingredient Strength | 500 mg/1 |
| Pharm Classes | Antimetabolite Immunosuppressant [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |
| Marketing Start Date | 1997-06-19 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA050723 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-06-19 |
| Marketing Category | NDA |
| Application Number | NDA050723 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-06-19 |
| Ingredient | Strength |
|---|---|
| MYCOPHENOLATE MOFETIL | 500 mg/1 |
| SPL SET ID: | 37241e87-4af4-4dc3-a1aa-ea6f20d8dc40 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0004-0259 | CellCept | Mycophenolate Mofetil |
| 0004-0260 | CellCept | Mycophenolate Mofetil |
| 0004-0261 | CellCept | Mycophenolate Mofetil |
| 0004-0298 | CellCept | Mycophenolate Mofetil hydrochloride |
| 21695-171 | CellCept | CellCept |
| 0054-0163 | Mycophenolate Mofetil | Mycophenolate Mofetil |
| 0054-0166 | Mycophenolate Mofetil | Mycophenolate Mofetil |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CELLCEPT 74357234 1889130 Live/Registered |
Hoffmann-La Roche Inc 1993-02-05 |