<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
69499-325-15
</NDCCode>
<PackageDescription>
15 TABLET, DELAYED RELEASE in 1 BOTTLE (69499-325-15)
</PackageDescription>
<NDC11Code>
69499-0325-15
</NDC11Code>
<ProductNDC>
69499-325
</ProductNDC>
<ProductTypeName>
HUMAN PRESCRIPTION DRUG
</ProductTypeName>
<ProprietaryName>
Doxycycline Hyclate
</ProprietaryName>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Doxycycline Hyclate
</NonProprietaryName>
<DosageFormName>
TABLET, DELAYED RELEASE
</DosageFormName>
<RouteName>
ORAL
</RouteName>
<StartMarketingDate>
20170620
</StartMarketingDate>
<EndMarketingDate/>
<MarketingCategoryName>
ANDA
</MarketingCategoryName>
<ApplicationNumber>
ANDA207494
</ApplicationNumber>
<LabelerName>
Solbuiomix
</LabelerName>
<SubstanceName>
DOXYCYCLINE HYCLATE
</SubstanceName>
<StrengthNumber>
200
</StrengthNumber>
<StrengthUnit>
mg/1
</StrengthUnit>
<Pharm_Classes/>
<DEASchedule/>
<Status>
Deprecated
</Status>
<LastUpdate>
2017-07-25
</LastUpdate>
<PackageNdcExcludeFlag/>
<ProductNdcExcludeFlag/>
<ListingRecordCertifiedThrough/>
<StartMarketingDatePackage/>
<EndMarketingDatePackage/>
<SamplePackage/>
</NDC>