<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
61786-213-08
</NDCCode>
<PackageDescription>
10 VIAL, GLASS in 1 VIAL (61786-213-08) > 10 mL in 1 VIAL, GLASS
</PackageDescription>
<NDC11Code>
61786-0213-08
</NDC11Code>
<ProductNDC>
61786-213
</ProductNDC>
<ProductTypeName>
HUMAN PRESCRIPTION DRUG
</ProductTypeName>
<ProprietaryName>
Furosemide
</ProprietaryName>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Furosemide
</NonProprietaryName>
<DosageFormName>
INJECTION, SOLUTION
</DosageFormName>
<RouteName>
INTRAVENOUS
</RouteName>
<StartMarketingDate>
20150307
</StartMarketingDate>
<EndMarketingDate/>
<MarketingCategoryName>
ANDA
</MarketingCategoryName>
<ApplicationNumber>
ANDA202747
</ApplicationNumber>
<LabelerName>
REMEDYREPACK INC.
</LabelerName>
<SubstanceName>
FUROSEMIDE
</SubstanceName>
<StrengthNumber>
10
</StrengthNumber>
<StrengthUnit>
mg/mL
</StrengthUnit>
<Pharm_Classes>
Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]
</Pharm_Classes>
<DEASchedule/>
<Status>
Deprecated
</Status>
<LastUpdate>
2017-03-20
</LastUpdate>
<PackageNdcExcludeFlag/>
<ProductNdcExcludeFlag/>
<ListingRecordCertifiedThrough/>
<StartMarketingDatePackage/>
<EndMarketingDatePackage/>
<SamplePackage/>
</NDC>