| NDC Code | 71288-803-92 |
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| Package Description | 4 VIAL, SINGLE-DOSE in 1 CARTON (71288-803-92) / 20 mL in 1 VIAL, SINGLE-DOSE (71288-803-91) |
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| Product NDC | 71288-803 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Mycophenolate Mofetil |
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| Non-Proprietary Name | Mycophenolate Mofetil |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20210115 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA212130 |
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| Manufacturer | Meitheal Pharmaceuticals Inc. |
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| Substance Name | MYCOPHENOLATE MOFETIL |
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| Strength | 500 |
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| Strength Unit | mg/20mL |
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| Pharmacy Classes | Antimetabolite Immunosuppressant [EPC] |
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