| NDC Code | 10122-210-02 |
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| Package Description | 1 VIAL, GLASS in 1 CARTON (10122-210-02) / 2.2 mL in 1 VIAL, GLASS |
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| Product NDC | 10122-210 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Myalept |
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| Non-Proprietary Name | Metreleptin |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | SUBCUTANEOUS |
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| Start Marketing Date | 20150305 |
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| Marketing Category Name | BLA |
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| Application Number | BLA125390 |
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| Manufacturer | Chiesi USA, Inc. |
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| Substance Name | METRELEPTIN |
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| Strength | 11.3 |
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| Strength Unit | mg/2.2mL |
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| Pharmacy Classes | Analogs/Derivatives [Chemical/Ingredient], Leptin Analog [EPC], Leptin [Chemical/Ingredient] |
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