<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
51645-606-01
</NDCCode>
<PackageDescription>
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51645-606-01)
</PackageDescription>
<NDC11Code>
51645-0606-01
</NDC11Code>
<ProductNDC>
51645-606
</ProductNDC>
<ProductTypeName>
HUMAN OTC DRUG
</ProductTypeName>
<ProprietaryName>
Docusate Sodium
</ProprietaryName>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Docusate Sodium
</NonProprietaryName>
<DosageFormName>
TABLET, FILM COATED
</DosageFormName>
<RouteName>
ORAL
</RouteName>
<StartMarketingDate>
20120330
</StartMarketingDate>
<EndMarketingDate>
20171130
</EndMarketingDate>
<MarketingCategoryName>
OTC MONOGRAPH NOT FINAL
</MarketingCategoryName>
<ApplicationNumber>
part334
</ApplicationNumber>
<LabelerName>
Gemini Pharmaceuticals, Inc. dba ONDRA Pharmaceuticals
</LabelerName>
<SubstanceName>
DOCUSATE SODIUM
</SubstanceName>
<StrengthNumber>
100
</StrengthNumber>
<StrengthUnit>
mg/1
</StrengthUnit>
<Pharm_Classes/>
<DEASchedule/>
<Status>
Deprecated
</Status>
<LastUpdate>
2017-12-07
</LastUpdate>
<PackageNdcExcludeFlag/>
<ProductNdcExcludeFlag/>
<ListingRecordCertifiedThrough/>
<StartMarketingDatePackage/>
<EndMarketingDatePackage/>
<SamplePackage/>
</NDC>