50742-359-21 : NDC 2026 Code

50742-359-21 : Progesterone ( Progesterone )

Additionally :

You can get information about “50742-359-21” NDC code in 50742-359-21 in HTML format

HTML | 50742-359-21 in TXT (Plain Text) format

TXT | 50742-359-21 in PDF (Portable Document Format)

PDF | 50742-359-21 in XML format

XML formats.

NDC Code : 50742-359-21 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "50742-359-21",
    "PackageDescription": "1 CARTON in 1 CARTON (50742-359-21)  / 21 BLISTER PACK in 1 CARTON (50742-359-07)  / 1 INSERT in 1 BLISTER PACK (50742-359-03) ",
    "NDC11Code": "50742-0359-21",
    "ProductNDC": "50742-359",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Progesterone",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Progesterone",
    "DosageFormName": "INSERT",
    "RouteName": "VAGINAL",
    "StartMarketingDate": "20261016",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA219588",
    "LabelerName": "Ingenus Pharmaceuticals, LLC",
    "SubstanceName": "PROGESTERONE",
    "StrengthNumber": "100",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Progesterone [CS], Progesterone [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2026-10-23",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20271231",
    "StartMarketingDatePackage": "20261016",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}