57587-294-01 : NDC 2026 Code

57587-294-01 : Buprenorphine Hydrochloride And Naloxone Hydrochloride ( )

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HTML | 57587-294-01 in TXT (Plain Text) format

TXT | 57587-294-01 in PDF (Portable Document Format)

PDF | 57587-294-01 in JSON format

JSON formats.

NDC Code : 57587-294-01 – XML Data Format

                    
<?xml version="1.0" encoding="UTF-8"?>
<NDC>
	<NDCCode>
		57587-294-01
	</NDCCode>
	<PackageDescription>
		1 BAG in 1 DRUM (57587-294-01)  &gt; 100000 TABLET in 1 BAG
	</PackageDescription>
	<NDC11Code>
		57587-0294-01
	</NDC11Code>
	<ProductNDC>
		57587-294
	</ProductNDC>
	<ProductTypeName>
		DRUG FOR FURTHER PROCESSING
	</ProductTypeName>
	<ProprietaryName/>
	<ProprietaryNameSuffix/>
	<NonProprietaryName>
		Buprenorphine Hydrochloride And Naloxone Hydrochloride
	</NonProprietaryName>
	<DosageFormName>
		TABLET
	</DosageFormName>
	<RouteName/>
	<StartMarketingDate>
		20160107
	</StartMarketingDate>
	<EndMarketingDate/>
	<MarketingCategoryName>
		DRUG FOR FURTHER PROCESSING
	</MarketingCategoryName>
	<ApplicationNumber/>
	<LabelerName>
		Ethypharm
	</LabelerName>
	<SubstanceName>
		BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
	</SubstanceName>
	<StrengthNumber>
		2; .5
	</StrengthNumber>
	<StrengthUnit>
		mg/1; mg/1
	</StrengthUnit>
	<Pharm_Classes/>
	<DEASchedule>
		CIII
	</DEASchedule>
	<Status>
		Deprecated
	</Status>
	<LastUpdate>
		2014-02-04
	</LastUpdate>
	<PackageNdcExcludeFlag/>
	<ProductNdcExcludeFlag/>
	<ListingRecordCertifiedThrough>
		20221231
	</ListingRecordCertifiedThrough>
	<StartMarketingDatePackage>
		01-NOV-21
	</StartMarketingDatePackage>
	<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>