68788-7702-2 : NDC 2026 Code

68788-7702-2 : Albuterol Sulfate ( Albuterol Sulfate )

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NDC Code : 68788-7702-2 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "68788-7702-2",
    "PackageDescription": "1 POUCH in 1 CARTON (68788-7702-2)  / 25 VIAL, SINGLE-DOSE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-DOSE",
    "NDC11Code": "68788-7702-02",
    "ProductNDC": "68788-7702",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Albuterol Sulfate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Albuterol Sulfate",
    "DosageFormName": "SOLUTION",
    "RouteName": "RESPIRATORY (INHALATION)",
    "StartMarketingDate": "20200501",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA074880",
    "LabelerName": "Preferred Pharmaceuticals, Inc.",
    "SubstanceName": "ALBUTEROL SULFATE",
    "StrengthNumber": "2.5",
    "StrengthUnit": "mg/3mL",
    "Pharm_Classes": "Adrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2026-02-13",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20200501",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}