<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
42808-500-16
</NDCCode>
<PackageDescription>
453.6 g in 1 JAR (42808-500-16)
</PackageDescription>
<NDC11Code>
42808-0500-16
</NDC11Code>
<ProductNDC>
42808-500
</ProductNDC>
<ProductTypeName>
HUMAN PRESCRIPTION DRUG
</ProductTypeName>
<ProprietaryName>
Sodium Polystyrene Sulfonate
</ProprietaryName>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Sodium Polystyrene Sulfonate
</NonProprietaryName>
<DosageFormName>
POWDER, FOR SUSPENSION
</DosageFormName>
<RouteName>
ORAL; RECTAL
</RouteName>
<StartMarketingDate>
20120401
</StartMarketingDate>
<EndMarketingDate>
20170831
</EndMarketingDate>
<MarketingCategoryName>
ANDA
</MarketingCategoryName>
<ApplicationNumber>
ANDA090313
</ApplicationNumber>
<LabelerName>
Exact-Rx, Inc.
</LabelerName>
<SubstanceName>
SODIUM POLYSTYRENE SULFONATE
</SubstanceName>
<StrengthNumber>
4.1
</StrengthNumber>
<StrengthUnit>
meq/g
</StrengthUnit>
<Pharm_Classes/>
<DEASchedule/>
<Status>
Deprecated
</Status>
<LastUpdate>
2017-09-01
</LastUpdate>
<PackageNdcExcludeFlag/>
<ProductNdcExcludeFlag/>
<ListingRecordCertifiedThrough/>
<StartMarketingDatePackage/>
<EndMarketingDatePackage/>
<SamplePackage/>
</NDC>