| NDC Code | 62238-008-04 |
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| Package Description | 1 POUCH in 1 BOX (62238-008-04) > 1 VIAL, GLASS in 1 POUCH (62238-008-01) > .5 g in 1 VIAL, GLASS |
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| Product NDC | 62238-008 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Raplixa |
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| Non-Proprietary Name | Fibrinogen Human And Thrombin Human |
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| Dosage Form | POWDER |
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| Usage | TOPICAL |
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| Start Marketing Date | 20150622 |
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| Marketing Category Name | BLA |
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| Application Number | BLA125523 |
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| Manufacturer | ProFibrix BV |
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| Substance Name | FIBRINOGEN HUMAN; HUMAN THROMBIN |
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| Strength | 79; 699 |
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| Strength Unit | mg/g; [iU]/g |
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| Pharmacy Classes | Human Blood Coagulation Factor [EPC],Increased Coagulation Activity [PE],Blood Coagulation Factors [Chemical/Ingredient],Human Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Blood Coagulation Factors [Chemical/Ingredient] |
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