dockets: FDA-2007-N-0475

Regulatory dockets from Regulations.gov — containers for related documents and comments in a rulemaking proceeding.

Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API

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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-2007-N-0475 FDA Midodrine Exclusivity Issues Nonrulemaking 2022-01-05T01:02:09Z 0b00006480439404         ["Exclusivity Issues", "Midodrine ", "CDER"] CDER Midodrine Exclusivity Issues     {"displayProperties": [{"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": ["Exclusivity Issues", "Midodrine ", "CDER"], "modifyDate": "2022-01-05T01:02:09Z", "dkAbstract": null, "agencyId": "FDA", "program": "CDER", "shortTitle": "Midodrine Exclusivity Issues", "subType2": null, "title": "Midodrine Exclusivity Issues", "generic": "N", "field1": null, "docketType": "Nonrulemaking", "petitionNbr": null, "rin": null, "organization": null, "legacyId": "2007N-0311", "subType": null, "category": null, "field2": "OPEN", "effectiveDate": null, "objectId": "0b00006480439404"} single_get

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