| NDC Code | 0004-0298-09 |
|---|
| Package Description | 4 VIAL in 1 CARTON (0004-0298-09) / 20 mL in 1 VIAL |
|---|
| Product NDC | 0004-0298 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Cellcept |
|---|
| Non-Proprietary Name | Mycophenolate Mofetil Hydrochloride |
|---|
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 19980812 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA050758 |
|---|
| Manufacturer | Genentech, Inc. |
|---|
| Substance Name | MYCOPHENOLATE MOFETIL HYDROCHLORIDE |
|---|
| Strength | 500 |
|---|
| Strength Unit | mg/20mL |
|---|
| Pharmacy Classes | Antimetabolite Immunosuppressant [EPC] |
|---|