| NDC Code | 17856-0595-5 |
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| Package Description | 1 CASE in 1 CUP, UNIT-DOSE (17856-0595-5) / 72 CUP, UNIT-DOSE in 1 CASE (17856-0595-1) / 15 mL in 1 CUP, UNIT-DOSE |
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| Product NDC | 17856-0595 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Sodium Citrate And Citric Acid |
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| Non-Proprietary Name | Sodium Citrate And Citric Acid Monohydrate |
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| Dosage Form | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 19690101 |
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| Marketing Category Name | UNAPPROVED DRUG OTHER |
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| Manufacturer | ATLANTIC BIOLOGICALS CORP. |
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| Substance Name | ANHYDROUS CITRIC ACID; SODIUM CITRATE |
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| Strength | 334; 500 |
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| Strength Unit | mg/5mL; mg/5mL |
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| Pharmacy Classes | Acidifying Activity [MoA], Acidifying Activity [MoA], Anti-coagulant [EPC], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE], Decreased Coagulation Factor Activity [PE] |
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