<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
59630-551-77
</NDCCode>
<PackageDescription>
1 DOSE PACK in 1 CARTON (59630-551-77) > 7 TABLET, FILM COATED in 1 DOSE PACK
</PackageDescription>
<NDC11Code>
59630-0551-77
</NDC11Code>
<ProductNDC>
59630-551
</ProductNDC>
<ProductTypeName>
HUMAN PRESCRIPTION DRUG
</ProductTypeName>
<ProprietaryName>
Mulpleta
</ProprietaryName>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Lusutrombopag
</NonProprietaryName>
<DosageFormName>
TABLET, FILM COATED
</DosageFormName>
<RouteName>
ORAL
</RouteName>
<StartMarketingDate>
20180827
</StartMarketingDate>
<EndMarketingDate/>
<MarketingCategoryName>
NDA
</MarketingCategoryName>
<ApplicationNumber>
NDA210923
</ApplicationNumber>
<LabelerName>
SHIONOGI INC.
</LabelerName>
<SubstanceName>
LUSUTROMBOPAG
</SubstanceName>
<StrengthNumber>
3
</StrengthNumber>
<StrengthUnit>
mg/1
</StrengthUnit>
<Pharm_Classes/>
<DEASchedule/>
<Status>
Active
</Status>
<LastUpdate>
2020-11-03
</LastUpdate>
<PackageNdcExcludeFlag>
N
</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>
N
</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>
20261231
</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>
20180827
</StartMarketingDatePackage>
<EndMarketingDatePackage/>
<SamplePackage>
Y
</SamplePackage>
</NDC>