53346-1201-2 : NDC 2026 Code

53346-1201-2 : Calcarea Phosphorica, Ferrum Phosphoricum, Kali Phosphoricum, Natrum Muriaticum ( Dr Reckeweg Bc-1 )

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PDF | 53346-1201-2 in JSON format

JSON formats.

NDC Code : 53346-1201-2 – XML Data Format

                    
<?xml version="1.0" encoding="UTF-8"?>
<NDC>
	<NDCCode>
		53346-1201-2
	</NDCCode>
	<PackageDescription>
		20 g in 1 BOTTLE (53346-1201-2)
	</PackageDescription>
	<NDC11Code>
		53346-1201-02
	</NDC11Code>
	<ProductNDC>
		53346-1201
	</ProductNDC>
	<ProductTypeName>
		HUMAN OTC DRUG
	</ProductTypeName>
	<ProprietaryName>
		Dr Reckeweg Bc-1
	</ProprietaryName>
	<ProprietaryNameSuffix>
		Combination Salt
	</ProprietaryNameSuffix>
	<NonProprietaryName>
		Calcarea Phosphorica, Ferrum Phosphoricum, Kali Phosphoricum, Natrum Muriaticum
	</NonProprietaryName>
	<DosageFormName>
		TABLET
	</DosageFormName>
	<RouteName>
		ORAL
	</RouteName>
	<StartMarketingDate>
		20120101
	</StartMarketingDate>
	<EndMarketingDate/>
	<MarketingCategoryName>
		UNAPPROVED HOMEOPATHIC
	</MarketingCategoryName>
	<ApplicationNumber/>
	<LabelerName>
		PHARMAZEUTISCHE FABRIK DR. RECKEWEG &amp; CO
	</LabelerName>
	<SubstanceName>
		FERROSOFERRIC PHOSPHATE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE; TRIBASIC CALCIUM PHOSPHATE
	</SubstanceName>
	<StrengthNumber>
		3; 3; 6; 3
	</StrengthNumber>
	<StrengthUnit>
		[hp_X]/20g; [hp_X]/20g; [hp_X]/20g; [hp_X]/20g
	</StrengthUnit>
	<Pharm_Classes/>
	<DEASchedule/>
	<Status>
		Deprecated
	</Status>
	<LastUpdate>
		2015-03-27
	</LastUpdate>
	<PackageNdcExcludeFlag/>
	<ProductNdcExcludeFlag/>
	<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>