{
"NDC": {
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"PackageDescription": "250 mL in 1 BOTTLE (43602-177-25) ",
"NDC11Code": "43602-0177-25",
"ProductNDC": "43602-177",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Methylphenidate Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Methylphenidate Hydrochloride",
"DosageFormName": "SOLUTION",
"RouteName": "ORAL",
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"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA207417",
"LabelerName": "Ascent Pharmaceuticals, Inc.",
"SubstanceName": "METHYLPHENIDATE",
"StrengthNumber": "5",
"StrengthUnit": "mg/5mL",
"Pharm_Classes": "Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE]",
"DEASchedule": "CII",
"Status": "Active",
"LastUpdate": "2021-02-20",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20210129",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}