68628-500-31 : NDC 2026 Code

68628-500-31 : Lucinactant ( Surfaxin )

Additionally :

You can get information about “68628-500-31” NDC code in 68628-500-31 in HTML format

HTML | 68628-500-31 in TXT (Plain Text) format

TXT | 68628-500-31 in PDF (Portable Document Format)

PDF | 68628-500-31 in XML format

XML formats.

NDC Code : 68628-500-31 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "68628-500-31",
    "PackageDescription": "1 VIAL, SINGLE-USE in 1 CARTON (68628-500-31)  &gt; 8.5 mL in 1 VIAL, SINGLE-USE",
    "NDC11Code": "68628-0500-31",
    "ProductNDC": "68628-500",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Surfaxin",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Lucinactant",
    "DosageFormName": "SUSPENSION",
    "RouteName": "ENDOTRACHEAL",
    "StartMarketingDate": "20131101",
    "EndMarketingDate": null,
    "MarketingCategoryName": "NDA",
    "ApplicationNumber": "NDA021746",
    "LabelerName": "Discovery Laboratories, Inc.",
    "SubstanceName": "COLFOSCERIL PALMITATE; 1-PALMITOYL-2-OLEOYL-SN-GLYCERO-3-(PHOSPHO-RAC-(1-GLYCEROL)), SODIUM SALT; PALMITIC ACID; SINAPULTIDE",
    "StrengthNumber": "22.5; 7.5; 4.05; .862",
    "StrengthUnit": "mg/mL; mg/mL; mg/mL; mg/mL",
    "Pharm_Classes": null,
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2017-01-05",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": null,
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}