81033-412-51 : NDC 2025 Code

81033-412-51 : Potassium Chloride ( Potassium Chloride )

Additionally :

You can get information about “81033-412-51” NDC code in 81033-412-51 in HTML format

HTML | 81033-412-51 in TXT (Plain Text) format

TXT | 81033-412-51 in PDF (Portable Document Format)

PDF | 81033-412-51 in XML format

XML formats.

NDC Code : 81033-412-51 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "81033-412-51",
    "PackageDescription": "50 CUP, UNIT-DOSE in 1 CASE (81033-412-51)  / 15 mL in 1 CUP, UNIT-DOSE (81033-412-15) ",
    "NDC11Code": "81033-0412-51",
    "ProductNDC": "81033-412",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Potassium Chloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Potassium Chloride",
    "DosageFormName": "SOLUTION",
    "RouteName": "ORAL",
    "StartMarketingDate": "20240610",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA216156",
    "LabelerName": "Kesin Pharma",
    "SubstanceName": "POTASSIUM CHLORIDE",
    "StrengthNumber": "20",
    "StrengthUnit": "meq/15mL",
    "Pharm_Classes": "Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2024-12-07",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20251231",
    "StartMarketingDatePackage": "20240610",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}