{
"NDC": {
"NDCCode": "63739-531-10",
"PackageDescription": "10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-531-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK",
"NDC11Code": "63739-0531-10",
"ProductNDC": "63739-531",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Cyclobenzaprine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Cyclobenzaprine Hydrochloride",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20070228",
"EndMarketingDate": "20210731",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA077797",
"LabelerName": "McKesson Corporation dba SKY Packaging",
"SubstanceName": "CYCLOBENZAPRINE HYDROCHLORIDE",
"StrengthNumber": "10",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2021-08-03",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20070228",
"EndMarketingDatePackage": "20210731",
"SamplePackage": "N"
}
}