<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
57664-437-33
</NDCCode>
<PackageDescription>
5000 TABLET in 1 BOTTLE (57664-437-33)
</PackageDescription>
<NDC11Code>
57664-0437-33
</NDC11Code>
<ProductNDC>
57664-437
</ProductNDC>
<ProductTypeName>
HUMAN PRESCRIPTION DRUG
</ProductTypeName>
<ProprietaryName>
Digoxin
</ProprietaryName>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Digoxin
</NonProprietaryName>
<DosageFormName>
TABLET
</DosageFormName>
<RouteName>
ORAL
</RouteName>
<StartMarketingDate>
20030731
</StartMarketingDate>
<EndMarketingDate/>
<MarketingCategoryName>
ANDA
</MarketingCategoryName>
<ApplicationNumber>
ANDA076363
</ApplicationNumber>
<LabelerName>
Caraco Pharmaceutical Laboratories, Ltd.
</LabelerName>
<SubstanceName>
DIGOXIN
</SubstanceName>
<StrengthNumber>
125
</StrengthNumber>
<StrengthUnit>
ug/1
</StrengthUnit>
<Pharm_Classes>
Cardiac Glycoside [EPC],Cardiac Glycosides [Chemical/Ingredient]
</Pharm_Classes>
<DEASchedule/>
<Status>
Deprecated
</Status>
<LastUpdate>
2015-02-27
</LastUpdate>
<PackageNdcExcludeFlag/>
<ProductNdcExcludeFlag/>
<ListingRecordCertifiedThrough/>
<StartMarketingDatePackage/>
<EndMarketingDatePackage/>
<SamplePackage/>
</NDC>