80425-0226-1 : NDC 2026 Code

80425-0226-1 : Depo-medrol, Lidocaine, Isopropyl Alcohol ( Multi-specialty Kit )

NDC Code : 80425-0226-1 – XML Data Format

                    
<?xml version="1.0" encoding="UTF-8"?>
<NDC>
	<NDCCode>
		80425-0226-1
	</NDCCode>
	<PackageDescription>
		1 KIT in 1 CARTON (80425-0226-1)  *  10 AMPULE in 1 CARTON (55150-158-72)  / 2 mL in 1 AMPULE *  5 mL in 1 POUCH *  25 VIAL, SINGLE-DOSE in 1 CARTON (70121-1573-5)  / 1 mL in 1 VIAL, SINGLE-DOSE
	</PackageDescription>
	<NDC11Code>
		80425-0226-01
	</NDC11Code>
	<ProductNDC>
		80425-0226
	</ProductNDC>
	<ProductTypeName>
		HUMAN PRESCRIPTION DRUG
	</ProductTypeName>
	<ProprietaryName>
		Multi-specialty Kit
	</ProprietaryName>
	<ProprietaryNameSuffix/>
	<NonProprietaryName>
		Depo-medrol, Lidocaine, Isopropyl Alcohol
	</NonProprietaryName>
	<DosageFormName>
		KIT
	</DosageFormName>
	<RouteName>
		INFILTRATION; INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; SOFT TISSUE; TOPICAL
	</RouteName>
	<StartMarketingDate>
		20230512
	</StartMarketingDate>
	<EndMarketingDate/>
	<MarketingCategoryName>
		UNAPPROVED DRUG OTHER
	</MarketingCategoryName>
	<ApplicationNumber/>
	<LabelerName>
		Advanced Rx Pharmacy of Tennessee, LLC
	</LabelerName>
	<SubstanceName/>
	<StrengthNumber/>
	<StrengthUnit/>
	<Pharm_Classes/>
	<DEASchedule/>
	<Status>
		Active
	</Status>
	<LastUpdate>
		2025-01-02
	</LastUpdate>
	<PackageNdcExcludeFlag>
		N
	</PackageNdcExcludeFlag>
	<ProductNdcExcludeFlag>
		N
	</ProductNdcExcludeFlag>
	<ListingRecordCertifiedThrough>
		20261231
	</ListingRecordCertifiedThrough>
	<StartMarketingDatePackage>
		20230512
	</StartMarketingDatePackage>
	<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>