<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
55045-3143-2
</NDCCode>
<PackageDescription>
20 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55045-3143-2)
</PackageDescription>
<NDC11Code>
55045-3143-02
</NDC11Code>
<ProductNDC>
55045-3143
</ProductNDC>
<ProductTypeName>
HUMAN OTC DRUG
</ProductTypeName>
<ProprietaryName>
Mucinex
</ProprietaryName>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Guaifenesin
</NonProprietaryName>
<DosageFormName>
TABLET, EXTENDED RELEASE
</DosageFormName>
<RouteName>
ORAL
</RouteName>
<StartMarketingDate>
20100512
</StartMarketingDate>
<EndMarketingDate/>
<MarketingCategoryName>
NDA
</MarketingCategoryName>
<ApplicationNumber>
NDA021282
</ApplicationNumber>
<LabelerName>
Dispensing Solutions, Inc.
</LabelerName>
<SubstanceName>
GUAIFENESIN
</SubstanceName>
<StrengthNumber>
600
</StrengthNumber>
<StrengthUnit>
mg/1
</StrengthUnit>
<Pharm_Classes/>
<DEASchedule/>
<Status>
Deprecated
</Status>
<LastUpdate>
2019-09-21
</LastUpdate>
<PackageNdcExcludeFlag/>
<ProductNdcExcludeFlag>
E
</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>
20171231
</ListingRecordCertifiedThrough>
<StartMarketingDatePackage/>
<EndMarketingDatePackage/>
<SamplePackage/>
</NDC>