{
"NDC": {
"NDCCode": "42023-145-01",
"PackageDescription": "100 CAPSULE in 1 BOTTLE (42023-145-01)",
"NDC11Code": "42023-0145-01",
"ProductNDC": "42023-145",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Dantrolene Sodium",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Dantrolene Sodium",
"DosageFormName": "CAPSULE",
"RouteName": "ORAL",
"StartMarketingDate": "20130408",
"EndMarketingDate": "20171031",
"MarketingCategoryName": "NDA AUTHORIZED GENERIC",
"ApplicationNumber": "NDA017443",
"LabelerName": "Par Pharmaceutical, Inc.",
"SubstanceName": "DANTROLENE SODIUM",
"StrengthNumber": "50",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Decreased Striated Muscle Contraction [PE],Decreased Striated Muscle Tone [PE],Skeletal Muscle Relaxant [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2017-11-01",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}