50580-506-02 : NDC 2026 Code

50580-506-02 : Acetaminophen And Diphenhydramine Hydrochloride ( Tylenol Pm )

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HTML | 50580-506-02 in TXT (Plain Text) format

TXT | 50580-506-02 in PDF (Portable Document Format)

PDF | 50580-506-02 in JSON format

JSON formats.

NDC Code : 50580-506-02 – XML Data Format

                    
<?xml version="1.0" encoding="UTF-8"?>
<NDC>
	<NDCCode>
		50580-506-02
	</NDCCode>
	<PackageDescription>
		2 TABLET, FILM COATED in 1 POUCH (50580-506-02) 
	</PackageDescription>
	<NDC11Code>
		50580-0506-02
	</NDC11Code>
	<ProductNDC>
		50580-506
	</ProductNDC>
	<ProductTypeName>
		HUMAN OTC DRUG
	</ProductTypeName>
	<ProprietaryName>
		Tylenol Pm
	</ProprietaryName>
	<ProprietaryNameSuffix>
		Extra Strength
	</ProprietaryNameSuffix>
	<NonProprietaryName>
		Acetaminophen And Diphenhydramine Hydrochloride
	</NonProprietaryName>
	<DosageFormName>
		TABLET, FILM COATED
	</DosageFormName>
	<RouteName>
		ORAL
	</RouteName>
	<StartMarketingDate>
		20140929
	</StartMarketingDate>
	<EndMarketingDate>
		20180930
	</EndMarketingDate>
	<MarketingCategoryName>
		OTC MONOGRAPH NOT FINAL
	</MarketingCategoryName>
	<ApplicationNumber>
		part343
	</ApplicationNumber>
	<LabelerName>
		Johnson &amp; Johnson Consumer Inc., McNeil Consumer Healthcare Division
	</LabelerName>
	<SubstanceName>
		ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
	</SubstanceName>
	<StrengthNumber>
		500; 25
	</StrengthNumber>
	<StrengthUnit>
		mg/1; mg/1
	</StrengthUnit>
	<Pharm_Classes/>
	<DEASchedule/>
	<Status>
		Deprecated
	</Status>
	<LastUpdate>
		2018-10-02
	</LastUpdate>
	<PackageNdcExcludeFlag>
		N
	</PackageNdcExcludeFlag>
	<ProductNdcExcludeFlag>
		N
	</ProductNdcExcludeFlag>
	<ListingRecordCertifiedThrough/>
	<StartMarketingDatePackage>
		20160128
	</StartMarketingDatePackage>
	<EndMarketingDatePackage>
		20180930
	</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>