54569-1280-0 : NDC 2025 Code

54569-1280-0 : Ascorbic Acid And Cholecalciferol And Sodium Fluoride And Vitamin A Palmitate ( Tri-vit With Fluoride Drops )

NDC Code : 54569-1280-0 – XML Data Format

                    
<?xml version="1.0" encoding="UTF-8"?>
<NDC>
	<NDCCode>
		54569-1280-0
	</NDCCode>
	<PackageDescription>
		1 BOTTLE, PLASTIC in 1 CARTON (54569-1280-0)  &gt; 50 mL in 1 BOTTLE, PLASTIC
	</PackageDescription>
	<NDC11Code>
		54569-1280-00
	</NDC11Code>
	<ProductNDC>
		54569-1280
	</ProductNDC>
	<ProductTypeName>
		HUMAN PRESCRIPTION DRUG
	</ProductTypeName>
	<ProprietaryName>
		Tri-vit With Fluoride Drops
	</ProprietaryName>
	<ProprietaryNameSuffix/>
	<NonProprietaryName>
		Ascorbic Acid And Cholecalciferol And Sodium Fluoride And Vitamin A Palmitate
	</NonProprietaryName>
	<DosageFormName>
		SOLUTION
	</DosageFormName>
	<RouteName>
		ORAL
	</RouteName>
	<StartMarketingDate>
		19950401
	</StartMarketingDate>
	<EndMarketingDate/>
	<MarketingCategoryName>
		UNAPPROVED DRUG OTHER
	</MarketingCategoryName>
	<ApplicationNumber/>
	<LabelerName>
		A-S Medication Solutions LLC
	</LabelerName>
	<SubstanceName>
		VITAMIN A PALMITATE; ASCORBIC ACID; CHOLECALCIFEROL; SODIUM FLUORIDE
	</SubstanceName>
	<StrengthNumber>
		1500; 35; 400; .25
	</StrengthNumber>
	<StrengthUnit>
		[iU]/mL; mg/mL; [iU]/mL; mg/mL
	</StrengthUnit>
	<Pharm_Classes>
		Vitamin A [Chemical/Ingredient],Vitamin A [EPC],Vitamin D [Chemical/Ingredient],Vitamin D [EPC]
	</Pharm_Classes>
	<DEASchedule/>
	<Status>
		Deprecated
	</Status>
	<LastUpdate>
		2018-01-10
	</LastUpdate>
	<PackageNdcExcludeFlag/>
	<ProductNdcExcludeFlag>
		E
	</ProductNdcExcludeFlag>
	<ListingRecordCertifiedThrough>
		20171231
	</ListingRecordCertifiedThrough>
	<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>