57664-710-88 : NDC 2026 Code

57664-710-88 : Methylphenidate Hydrochloride ( Methylphenidate Hydrochloride )

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NDC Code : 57664-710-88 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "57664-710-88",
    "PackageDescription": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-710-88) ",
    "NDC11Code": "57664-0710-88",
    "ProductNDC": "57664-710",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Methylphenidate Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Methylphenidate Hydrochloride",
    "DosageFormName": "TABLET, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20241220",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA217229",
    "LabelerName": "Sun Pharmaceutical Industries, Inc.",
    "SubstanceName": "METHYLPHENIDATE HYDROCHLORIDE",
    "StrengthNumber": "72",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE]",
    "DEASchedule": "CII",
    "Status": "Active",
    "LastUpdate": "2024-12-21",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20241220",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}