60687-260-69 : NDC 2026 Code

60687-260-69 : Ranitidine Hydrochloride ( Ranitidine )

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NDC Code : 60687-260-69 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "60687-260-69",
    "PackageDescription": "5 TRAY in 1 CASE (60687-260-69)  &gt; 10 CUP, UNIT-DOSE in 1 TRAY (60687-260-48)  &gt; 10 mL in 1 CUP, UNIT-DOSE (60687-260-42) ",
    "NDC11Code": "60687-0260-69",
    "ProductNDC": "60687-260",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Ranitidine",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Ranitidine Hydrochloride",
    "DosageFormName": "SOLUTION",
    "RouteName": "ORAL",
    "StartMarketingDate": "20171107",
    "EndMarketingDate": "20210531",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA091288",
    "LabelerName": "American Health Packaging",
    "SubstanceName": "RANITIDINE HYDROCHLORIDE",
    "StrengthNumber": "15",
    "StrengthUnit": "mg/mL",
    "Pharm_Classes": "Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2021-06-02",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20171107",
    "EndMarketingDatePackage": "20210531",
    "SamplePackage": "N"
  }
}