<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
75872-0001-1
</NDCCode>
<PackageDescription>
2 g in 1 VIAL (75872-0001-1)
</PackageDescription>
<NDC11Code>
75872-0001-01
</NDC11Code>
<ProductNDC>
75872-0001
</ProductNDC>
<ProductTypeName>
BULK INGREDIENT
</ProductTypeName>
<ProprietaryName/>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Tafluprost
</NonProprietaryName>
<DosageFormName>
SOLUTION
</DosageFormName>
<RouteName/>
<StartMarketingDate>
20110615
</StartMarketingDate>
<EndMarketingDate/>
<MarketingCategoryName>
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
</MarketingCategoryName>
<ApplicationNumber/>
<LabelerName>
AGC Inc.
</LabelerName>
<SubstanceName>
TAFLUPROST
</SubstanceName>
<StrengthNumber>
2
</StrengthNumber>
<StrengthUnit>
g/2g
</StrengthUnit>
<Pharm_Classes/>
<DEASchedule/>
<Status>
Unfinished
</Status>
<LastUpdate>
2025-12-19
</LastUpdate>
<PackageNdcExcludeFlag/>
<ProductNdcExcludeFlag/>
<ListingRecordCertifiedThrough>
20261231
</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>
15-JUN-11
</StartMarketingDatePackage>
<EndMarketingDatePackage/>
<SamplePackage/>
</NDC>