<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
49580-4560-4
</NDCCode>
<PackageDescription>
24 BOTTLE in 1 CASE (49580-4560-4) > 237 mL in 1 BOTTLE
</PackageDescription>
<NDC11Code>
49580-4560-04
</NDC11Code>
<ProductNDC>
49580-4560
</ProductNDC>
<ProductTypeName>
HUMAN OTC DRUG
</ProductTypeName>
<ProprietaryName/>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Ibuprofen
</NonProprietaryName>
<DosageFormName>
SUSPENSION
</DosageFormName>
<RouteName/>
<StartMarketingDate>
20200326
</StartMarketingDate>
<EndMarketingDate/>
<MarketingCategoryName>
DRUG FOR FURTHER PROCESSING
</MarketingCategoryName>
<ApplicationNumber/>
<LabelerName>
P & L Development, LLC
</LabelerName>
<SubstanceName>
IBUPROFEN
</SubstanceName>
<StrengthNumber>
100
</StrengthNumber>
<StrengthUnit>
mg/5mL
</StrengthUnit>
<Pharm_Classes/>
<DEASchedule/>
<Status>
Deprecated
</Status>
<LastUpdate>
2014-02-04
</LastUpdate>
<PackageNdcExcludeFlag/>
<ProductNdcExcludeFlag/>
<ListingRecordCertifiedThrough>
20211231
</ListingRecordCertifiedThrough>
<StartMarketingDatePackage/>
<EndMarketingDatePackage/>
<SamplePackage/>
</NDC>