dockets: FDA-2013-P-1609

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id agency_id title docket_type last_modified object_id rin dkabstract category subtype keywords program short_title effective_date organization attrs_raw attr_source
FDA-2013-P-1609 FDA Determine Whether the two-Vial Container Closure System That was Previously Used to Package the Following Lupron Depot (Leuprolide Acetate for Depot Suspension) Injection Drug Products was Voluntarily Withdrawn From Sale for Safety or Efficacy Nonrulemaking 2014-12-05T11:34:23Z 0b000064814ba5cf   Closed via FR Notice     ["CDER", "Citizen Petition", "2013-10152", "OPEN", "Lachman", "Lupron Depot", "Leuprolide Acetate", "Depot Suspension", "ANDA"] CDER Determine Whether the two-Vial Container Closure System That was Previously Used to Package Lupron Depot Injection Drug Products was Voluntarily Withdrawn From Sale for Safety or Efficacy     {"displayProperties": [{"name": "abstract", "label": "General Information", "tooltip": "Describes an agency's specific regulatory action; equivalents: Abstract, Description, Docket Subject, Related To, Summary."}, {"name": "legacyId", "label": "Legacy ID", "tooltip": "A pre-FDMS agency specific identifier migrated from a legacy system."}, {"name": "generic", "label": "Docket Item Code", "tooltip": "An agency specific code that identifies the type of document that established the docket (regulatory action)."}, {"name": "program", "label": "Center", "tooltip": "The agency specific program associated with the docket (regulatory action); equivalents: Docket Item Code, Location."}, {"name": "field2", "label": "Docket Status", "tooltip": "Used to Identity that a Docket's Status is Open or Closed"}, {"name": "shortTitle", "label": "Short Title", "tooltip": "A combination of letters and or numbers assigned to an agency's regulatory action for purposes of brevity."}], "keywords": ["CDER", "Citizen Petition", "2013-10152", "OPEN", "Lachman", "Lupron Depot", "Leuprolide Acetate", "Depot Suspension", "ANDA"], "modifyDate": "2014-12-05T11:34:23Z", "dkAbstract": "Closed via FR Notice", "agencyId": "FDA", "program": "CDER", "shortTitle": "Determine Whether the two-Vial Container Closure System That was Previously Used to Package Lupron Depot Injection Drug Products was Voluntarily Withdrawn From Sale for Safety or Efficacy", "subType2": null, "title": "Determine Whether the two-Vial Container Closure System That was Previously Used to Package the Following Lupron Depot (Leuprolide Acetate for Depot Suspension) Injection Drug Products was Voluntarily Withdrawn From Sale for Safety or Efficacy", "generic": "P", "field1": null, "docketType": "Nonrulemaking", "petitionNbr": null, "rin": null, "organization": null, "legacyId": "2013-10152", "subType": null, "category": null, "field2": "Closed", "effectiveDate": null, "objectId": "0b000064814ba5cf"} single_get

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