<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
49281-912-03
</NDCCode>
<PackageDescription>
1 VIAL, MULTI-DOSE in 1 PACKAGE (49281-912-03) > 3 mL in 1 VIAL, MULTI-DOSE (49281-912-68)
</PackageDescription>
<NDC11Code>
49281-0912-03
</NDC11Code>
<ProductNDC>
49281-912
</ProductNDC>
<ProductTypeName>
VACCINE
</ProductTypeName>
<ProprietaryName>
Sodium Chloride
</ProprietaryName>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Sodium Chloride
</NonProprietaryName>
<DosageFormName>
INJECTION
</DosageFormName>
<RouteName>
SUBCUTANEOUS
</RouteName>
<StartMarketingDate>
19530522
</StartMarketingDate>
<EndMarketingDate/>
<MarketingCategoryName>
BLA
</MarketingCategoryName>
<ApplicationNumber>
BLA103915
</ApplicationNumber>
<LabelerName>
Sanofi Pasteur Inc.
</LabelerName>
<SubstanceName/>
<StrengthNumber/>
<StrengthUnit/>
<Pharm_Classes/>
<DEASchedule/>
<Status>
Deprecated
</Status>
<LastUpdate>
2016-12-02
</LastUpdate>
<PackageNdcExcludeFlag/>
<ProductNdcExcludeFlag/>
<ListingRecordCertifiedThrough/>
<StartMarketingDatePackage/>
<EndMarketingDatePackage/>
<SamplePackage/>
</NDC>