32909-727-01 : NDC 2026 Code

32909-727-01 : Barium Sulfate ( E-z-cat Dry )

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HTML | 32909-727-01 in TXT (Plain Text) format

TXT | 32909-727-01 in PDF (Portable Document Format)

PDF | 32909-727-01 in JSON format

JSON formats.

NDC Code : 32909-727-01 – XML Data Format

                    
<?xml version="1.0" encoding="UTF-8"?>
<NDC>
	<NDCCode>
		32909-727-01
	</NDCCode>
	<PackageDescription>
		50 POUCH in 1 BOX (32909-727-01)  &gt; 23 g in 1 POUCH
	</PackageDescription>
	<NDC11Code>
		32909-0727-01
	</NDC11Code>
	<ProductNDC>
		32909-727
	</ProductNDC>
	<ProductTypeName>
		HUMAN PRESCRIPTION DRUG
	</ProductTypeName>
	<ProprietaryName>
		E-z-cat Dry
	</ProprietaryName>
	<ProprietaryNameSuffix/>
	<NonProprietaryName>
		Barium Sulfate
	</NonProprietaryName>
	<DosageFormName>
		POWDER, FOR SUSPENSION
	</DosageFormName>
	<RouteName>
		ORAL
	</RouteName>
	<StartMarketingDate>
		19960101
	</StartMarketingDate>
	<EndMarketingDate>
		20190601
	</EndMarketingDate>
	<MarketingCategoryName>
		UNAPPROVED DRUG OTHER
	</MarketingCategoryName>
	<ApplicationNumber/>
	<LabelerName>
		E-Z-EM Canada Inc
	</LabelerName>
	<SubstanceName>
		BARIUM SULFATE
	</SubstanceName>
	<StrengthNumber>
		9.5
	</StrengthNumber>
	<StrengthUnit>
		g/23g
	</StrengthUnit>
	<Pharm_Classes>
		Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA]
	</Pharm_Classes>
	<DEASchedule/>
	<Status>
		Deprecated
	</Status>
	<LastUpdate>
		2019-06-04
	</LastUpdate>
	<PackageNdcExcludeFlag>
		N
	</PackageNdcExcludeFlag>
	<ProductNdcExcludeFlag>
		N
	</ProductNdcExcludeFlag>
	<ListingRecordCertifiedThrough/>
	<StartMarketingDatePackage>
		19960101
	</StartMarketingDatePackage>
	<EndMarketingDatePackage>
		20190601
	</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>