| NDC Code | 50242-245-86 |
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| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (50242-245-86) / 15 mL in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 50242-245 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Phesgo |
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| Non-Proprietary Name | Pertuzumab, Trastuzumab, And Hyaluronidase-zzxf |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | SUBCUTANEOUS |
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| Start Marketing Date | 20200629 |
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| Marketing Category Name | BLA |
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| Application Number | BLA761170 |
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| Manufacturer | Genentech, Inc. |
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| Substance Name | HYALURONIDASE (HUMAN RECOMBINANT); PERTUZUMAB; TRASTUZUMAB |
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| Strength | 30000; 1200; 600 |
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| Strength Unit | U/15mL; mg/15mL; mg/15mL |
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| Pharmacy Classes | Endoglycosidase [EPC], Glycoside Hydrolases [CS], HER2/Neu/cerbB2 Antagonists [MoA], HER2/Neu/cerbB2 Antagonists [MoA], HER2/neu Receptor Antagonist [EPC], HER2/neu Receptor Antagonist [EPC] |
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