{
"NDC": {
"NDCCode": "62756-873-18",
"PackageDescription": "1000 CAPSULE in 1 BOTTLE (62756-873-18)",
"NDC11Code": "62756-0873-18",
"ProductNDC": "62756-873",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Valproic Acid",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Valproic Acid",
"DosageFormName": "CAPSULE",
"RouteName": "ORAL",
"StartMarketingDate": "20130228",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA091037",
"LabelerName": "Sun Pharmaceutical Industries Limited",
"SubstanceName": "VALPROIC ACID",
"StrengthNumber": "250",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2017-02-13",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}