<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
68084-785-21
</NDCCode>
<PackageDescription>
30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-785-21) > 1 TABLET in 1 BLISTER PACK (68084-785-11)
</PackageDescription>
<NDC11Code>
68084-0785-21
</NDC11Code>
<ProductNDC>
68084-785
</ProductNDC>
<ProductTypeName>
HUMAN PRESCRIPTION DRUG
</ProductTypeName>
<ProprietaryName>
Doxycycline Monohydrate
</ProprietaryName>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Doxycycline
</NonProprietaryName>
<DosageFormName>
TABLET
</DosageFormName>
<RouteName>
ORAL
</RouteName>
<StartMarketingDate>
20141215
</StartMarketingDate>
<EndMarketingDate>
20161231
</EndMarketingDate>
<MarketingCategoryName>
ANDA
</MarketingCategoryName>
<ApplicationNumber>
ANDA065070
</ApplicationNumber>
<LabelerName>
American Health Packaging
</LabelerName>
<SubstanceName>
DOXYCYCLINE
</SubstanceName>
<StrengthNumber>
100
</StrengthNumber>
<StrengthUnit>
mg/1
</StrengthUnit>
<Pharm_Classes/>
<DEASchedule/>
<Status>
Deprecated
</Status>
<LastUpdate>
2017-01-05
</LastUpdate>
<PackageNdcExcludeFlag/>
<ProductNdcExcludeFlag/>
<ListingRecordCertifiedThrough/>
<StartMarketingDatePackage/>
<EndMarketingDatePackage/>
<SamplePackage/>
</NDC>