{
"NDC": {
"NDCCode": "17856-0792-6",
"PackageDescription": "72 CUP in 1 BOX, UNIT-DOSE (17856-0792-6) / 5 mL in 1 CUP (17856-0792-5) ",
"NDC11Code": "17856-0792-06",
"ProductNDC": "17856-0792",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Valproic Acid",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Valproic Acid",
"DosageFormName": "SOLUTION",
"RouteName": "ORAL",
"StartMarketingDate": "19950113",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA074060",
"LabelerName": "ATLANTIC BIOLOGICALS CORP.",
"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": "2024-11-30",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20251231",
"StartMarketingDatePackage": "20230201",
"EndMarketingDatePackage": "20241129",
"SamplePackage": "N"
}
}