{
"NDC": {
"NDCCode": "70518-1968-0",
"PackageDescription": "10 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (70518-1968-0) > 12.5 mL in 1 CUP, UNIT-DOSE (70518-1968-1) ",
"NDC11Code": "70518-1968-00",
"ProductNDC": "70518-1968",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Valproic Acid",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Valproic Acid",
"DosageFormName": "SOLUTION",
"RouteName": "ORAL",
"StartMarketingDate": "20190320",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA075379",
"LabelerName": "REMEDYREPACK INC.",
"SubstanceName": "VALPROIC ACID",
"StrengthNumber": "250",
"StrengthUnit": "mg/5mL",
"Pharm_Classes": "Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2021-01-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20201231",
"StartMarketingDatePackage": "20190320",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}