50844-529-08 : NDC 2026 Code

50844-529-08 : Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hbr, Phenylephrine Hcl ( Cold Relief )

NDC Code : 50844-529-08 – XML Data Format

                    
<?xml version="1.0" encoding="UTF-8"?>
<NDC>
	<NDCCode>
		50844-529-08
	</NDCCode>
	<PackageDescription>
		1 KIT in 1 CARTON (50844-529-08)  *  12 TABLET, FILM COATED in 1 BLISTER PACK *  12 TABLET, FILM COATED in 1 BLISTER PACK
	</PackageDescription>
	<NDC11Code>
		50844-0529-08
	</NDC11Code>
	<ProductNDC>
		50844-529
	</ProductNDC>
	<ProductTypeName>
		HUMAN OTC DRUG
	</ProductTypeName>
	<ProprietaryName>
		Cold Relief
	</ProprietaryName>
	<ProprietaryNameSuffix>
		Multi-symptom
	</ProprietaryNameSuffix>
	<NonProprietaryName>
		Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hbr, Phenylephrine Hcl
	</NonProprietaryName>
	<DosageFormName>
		KIT
	</DosageFormName>
	<RouteName/>
	<StartMarketingDate>
		20050721
	</StartMarketingDate>
	<EndMarketingDate>
		20221124
	</EndMarketingDate>
	<MarketingCategoryName>
		OTC MONOGRAPH FINAL
	</MarketingCategoryName>
	<ApplicationNumber>
		part341
	</ApplicationNumber>
	<LabelerName>
		L.N.K. International, Inc.
	</LabelerName>
	<SubstanceName/>
	<StrengthNumber/>
	<StrengthUnit/>
	<Pharm_Classes/>
	<DEASchedule/>
	<Status>
		Deprecated
	</Status>
	<LastUpdate>
		2022-11-24
	</LastUpdate>
	<PackageNdcExcludeFlag>
		N
	</PackageNdcExcludeFlag>
	<ProductNdcExcludeFlag>
		N
	</ProductNdcExcludeFlag>
	<ListingRecordCertifiedThrough/>
	<StartMarketingDatePackage>
		20050721
	</StartMarketingDatePackage>
	<EndMarketingDatePackage>
		20221124
	</EndMarketingDatePackage>
	<SamplePackage>
		N
	</SamplePackage>
</NDC>

                    
                

NDC XML XSD Schema

                    
<xs:schema attributeFormDefault="unqualified" elementFormDefault="qualified" xmlns:xs="http://www.w3.org/2001/XMLSchema">
  <xs:element name="NDC">
    <xs:complexType>
      <xs:sequence>
        <xs:element type="xs:string" name="NDCCode"/>
        <xs:element type="xs:string" name="PackageDescription"/>
        <xs:element type="xs:string" name="NDC11Code"/>
        <xs:element type="xs:string" name="ProductNDC"/>
        <xs:element type="xs:string" name="ProductTypeName"/>
        <xs:element type="xs:string" name="ProprietaryName"/>
        <xs:element type="xs:string" name="ProprietaryNameSuffix"/>
        <xs:element type="xs:string" name="NonProprietaryName"/>
        <xs:element type="xs:string" name="DosageFormName"/>
        <xs:element type="xs:string" name="RouteName"/>
        <xs:element type="xs:string" name="StartMarketingDate"/>
        <xs:element type="xs:string" name="EndMarketingDate"/>
        <xs:element type="xs:string" name="MarketingCategoryName"/>
        <xs:element type="xs:string" name="ApplicationNumber"/>
        <xs:element type="xs:string" name="LabelerName"/>
        <xs:element type="xs:string" name="SubstanceName"/>
        <xs:element type="xs:string" name="StrengthNumber"/>
        <xs:element type="xs:string" name="StrengthUnit"/>
        <xs:element type="xs:string" name="Pharm_Classes"/>
        <xs:element type="xs:string" name="DEASchedule"/>
        <xs:element type="xs:string" name="Status"/>
        <xs:element type="xs:string" name="LastUpdate"/>
        <xs:element type="xs:string" name="PackageNdcExcludeFlag"/>
        <xs:element type="xs:string" name="ProductNdcExcludeFlag"/>
        <xs:element type="xs:string" name="ListingRecordCertifiedThrough"/>
        <xs:element type="xs:string" name="StartMarketingDatePackage"/>
        <xs:element type="xs:string" name="EndMarketingDatePackage"/>
        <xs:element type="xs:string" name="SamplePackage"/>
      </xs:sequence>
    </xs:complexType>
  </xs:element>
</xs:schema>