| NDC Code | 60687-834-76 |
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| Package Description | 10 TRAY in 1 CASE (60687-834-76) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-834-51) / 30 mL in 1 CUP, UNIT-DOSE (60687-834-45) |
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| Product NDC | 60687-834 |
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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 | 20240721 |
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| Marketing Category Name | UNAPPROVED DRUG OTHER |
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| Manufacturer | American Health Packaging |
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| Substance Name | ANHYDROUS CITRIC ACID; SODIUM CITRATE, UNSPECIFIED FORM |
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| Strength | 2004; 3000 |
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| Strength Unit | mg/30mL; mg/30mL |
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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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