| NDC Code | 54288-141-04 |
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| Package Description | 4 VIAL in 1 CARTON (54288-141-04) / 20 mL in 1 VIAL |
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| Product NDC | 54288-141 |
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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 Hydrochloride |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20230308 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA214283 |
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| Manufacturer | BPI Labs LLC |
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| Substance Name | MYCOPHENOLATE MOFETIL HYDROCHLORIDE |
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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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