| NDC Code | 81839-782-02 |
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| Package Description | 30 BAG in 1 CARTON (81839-782-02) / 250 mL in 1 BAG (81839-782-01) |
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| Product NDC | 81839-782 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Anticoagulant Sodium Citrate |
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| Non-Proprietary Name | Trisodium Citrate Dihydrate |
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| Dosage Form | SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20220701 |
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| Marketing Category Name | ANDA |
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| Application Number | BA125750 |
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| Manufacturer | CSL Plasma Inc. |
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| Substance Name | TRISODIUM CITRATE DIHYDRATE |
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| Strength | 40 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE] |
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