{
"NDC": {
"NDCCode": "68084-952-25",
"PackageDescription": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-952-25) / 1 TABLET in 1 BLISTER PACK (68084-952-95) ",
"NDC11Code": "68084-0952-25",
"ProductNDC": "68084-952",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Albuterol Sulfate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Albuterol Sulfate",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20151008",
"EndMarketingDate": "20250131",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA072637",
"LabelerName": "American Health Packaging",
"SubstanceName": "ALBUTEROL SULFATE",
"StrengthNumber": "4",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Adrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2025-02-04",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20151008",
"EndMarketingDatePackage": "20250131",
"SamplePackage": "N"
}
}