43742-0229-1 : NDC 2026 Code

43742-0229-1 : Phytolacca Decandra, Trifolium Pratense, Hepar Sulphuris Calcareum, Silicea, Thymus, Conium Maculatum ( )

NDC Code : 43742-0229-1 – XML Data Format

                    
<?xml version="1.0" encoding="UTF-8"?>
<NDC>
	<NDCCode>
		43742-0229-1
	</NDCCode>
	<PackageDescription>
		960 mL in 1 BOTTLE (43742-0229-1) 
	</PackageDescription>
	<NDC11Code>
		43742-0229-01
	</NDC11Code>
	<ProductNDC>
		43742-0229
	</ProductNDC>
	<ProductTypeName>
		DRUG FOR FURTHER PROCESSING
	</ProductTypeName>
	<ProprietaryName/>
	<ProprietaryNameSuffix/>
	<NonProprietaryName>
		Phytolacca Decandra, Trifolium Pratense, Hepar Sulphuris Calcareum, Silicea, Thymus, Conium Maculatum
	</NonProprietaryName>
	<DosageFormName>
		LIQUID
	</DosageFormName>
	<RouteName/>
	<StartMarketingDate>
		20130430
	</StartMarketingDate>
	<EndMarketingDate>
		20250603
	</EndMarketingDate>
	<MarketingCategoryName>
		DRUG FOR FURTHER PROCESSING
	</MarketingCategoryName>
	<ApplicationNumber/>
	<LabelerName>
		Deseret Biologicals, Inc.
	</LabelerName>
	<SubstanceName>
		CALCIUM SULFIDE; CONIUM MACULATUM FLOWERING TOP; PHYTOLACCA AMERICANA ROOT; SILICON DIOXIDE; SUS SCROFA THYMUS; TRIFOLIUM PRATENSE FLOWER
	</SubstanceName>
	<StrengthNumber>
		8; 12; 6; 8; 8; 6
	</StrengthNumber>
	<StrengthUnit>
		[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
	</StrengthUnit>
	<Pharm_Classes/>
	<DEASchedule/>
	<Status>
		Deprecated
	</Status>
	<LastUpdate>
		2014-02-04
	</LastUpdate>
	<PackageNdcExcludeFlag/>
	<ProductNdcExcludeFlag/>
	<ListingRecordCertifiedThrough/>
	<StartMarketingDatePackage>
		30-APR-13
	</StartMarketingDatePackage>
	<EndMarketingDatePackage>
		03-JUN-25
	</EndMarketingDatePackage>
	<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>