{
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"PackageDescription": "25 VIAL in 1 CARTON (70095-050-03) / 50 mL in 1 VIAL (70095-050-01) ",
"NDC11Code": "70095-0050-03",
"ProductNDC": "70095-050",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Sodium Bicarbonate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Sodium Bicarbonate",
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"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA217594",
"LabelerName": "Sun Pharmaceutical Industries Limited",
"SubstanceName": "SODIUM BICARBONATE",
"StrengthNumber": "84",
"StrengthUnit": "mg/mL",
"Pharm_Classes": "Alkalinizing Activity [MoA]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2024-03-16",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20240315",
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"SamplePackage": "N"
}
}