{
"NDC": {
"NDCCode": "60687-953-56",
"PackageDescription": "10 TRAY in 1 CASE (60687-953-56) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-953-48) / 10 mL in 1 CUP, UNIT-DOSE (60687-953-42) ",
"NDC11Code": "60687-0953-56",
"ProductNDC": "60687-953",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Valproic Acid",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Valproic Acid",
"DosageFormName": "SOLUTION",
"RouteName": "ORAL",
"StartMarketingDate": "20260804",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA075379",
"LabelerName": "American Health Packaging",
"SubstanceName": "VALPROIC ACID",
"StrengthNumber": "500",
"StrengthUnit": "mg/10mL",
"Pharm_Classes": "Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2026-08-05",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20271231",
"StartMarketingDatePackage": "20260804",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}