60885-0050-0 : NDC 2026 Code

60885-0050-0 : Timolol Maleate ( )

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TXT | 60885-0050-0 in PDF (Portable Document Format)

PDF | 60885-0050-0 in JSON format

JSON formats.

NDC Code : 60885-0050-0 – XML Data Format

                    
<?xml version="1.0" encoding="UTF-8"?>
<NDC>
	<NDCCode>
		60885-0050-0
	</NDCCode>
	<PackageDescription>
		32 PACKET in 1 CARTON (60885-0050-0)  &gt; 4 POUCH in 1 PACKET &gt; 3 BLISTER PACK in 1 POUCH &gt; 5 APPLICATOR in 1 BLISTER PACK &gt; .2 mL in 1 APPLICATOR
	</PackageDescription>
	<NDC11Code>
		60885-0050-00
	</NDC11Code>
	<ProductNDC>
		60885-0050
	</ProductNDC>
	<ProductTypeName>
		BULK INGREDIENT
	</ProductTypeName>
	<ProprietaryName/>
	<ProprietaryNameSuffix/>
	<NonProprietaryName>
		Timolol Maleate
	</NonProprietaryName>
	<DosageFormName>
		SOLUTION/ DROPS
	</DosageFormName>
	<RouteName/>
	<StartMarketingDate>
		20090217
	</StartMarketingDate>
	<EndMarketingDate>
		20140818
	</EndMarketingDate>
	<MarketingCategoryName>
		DRUG FOR FURTHER PROCESSING
	</MarketingCategoryName>
	<ApplicationNumber/>
	<LabelerName>
		Laboratoires Merck Sharp &amp; Dohme-Chibret
	</LabelerName>
	<SubstanceName>
		TIMOLOL MALEATE
	</SubstanceName>
	<StrengthNumber>
		.25
	</StrengthNumber>
	<StrengthUnit>
		g/100mL
	</StrengthUnit>
	<Pharm_Classes/>
	<DEASchedule/>
	<Status>
		Deprecated
	</Status>
	<LastUpdate>
		2014-02-04
	</LastUpdate>
	<PackageNdcExcludeFlag/>
	<ProductNdcExcludeFlag/>
	<ListingRecordCertifiedThrough>
		20140818
	</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>