<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
60687-834-76
</NDCCode>
<PackageDescription>
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)
</PackageDescription>
<NDC11Code>
60687-0834-76
</NDC11Code>
<ProductNDC>
60687-834
</ProductNDC>
<ProductTypeName>
HUMAN PRESCRIPTION DRUG
</ProductTypeName>
<ProprietaryName>
Sodium Citrate And Citric Acid
</ProprietaryName>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Sodium Citrate And Citric Acid Monohydrate
</NonProprietaryName>
<DosageFormName>
SOLUTION
</DosageFormName>
<RouteName>
ORAL
</RouteName>
<StartMarketingDate>
20240721
</StartMarketingDate>
<EndMarketingDate/>
<MarketingCategoryName>
UNAPPROVED DRUG OTHER
</MarketingCategoryName>
<ApplicationNumber/>
<LabelerName>
American Health Packaging
</LabelerName>
<SubstanceName>
ANHYDROUS CITRIC ACID; SODIUM CITRATE, UNSPECIFIED FORM
</SubstanceName>
<StrengthNumber>
2004; 3000
</StrengthNumber>
<StrengthUnit>
mg/30mL; mg/30mL
</StrengthUnit>
<Pharm_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]
</Pharm_Classes>
<DEASchedule/>
<Status>
Active
</Status>
<LastUpdate>
2024-07-23
</LastUpdate>
<PackageNdcExcludeFlag>
N
</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>
N
</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>
20261231
</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>
20240721
</StartMarketingDatePackage>
<EndMarketingDatePackage/>
<SamplePackage>
N
</SamplePackage>
</NDC>