dockets: FDA-2013-N-1615

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

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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-N-1615	FDA	Draft Generic Drug User Fee Act Information Technology Plan; Availability for Comment	Nonrulemaking	2014-02-26T07:29:46Z	0b000064814baa40					["cder", "cder2013220", "open"]	CDER				{"displayProperties": [{"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"}], "keywords": ["cder", "cder2013220", "open"], "modifyDate": "2014-02-26T07:29:46Z", "dkAbstract": null, "agencyId": "FDA", "program": "CDER", "shortTitle": null, "subType2": null, "title": "Draft Generic Drug User Fee Act Information Technology Plan; Availability for Comment", "generic": "N", "field1": null, "docketType": "Nonrulemaking", "petitionNbr": null, "rin": null, "organization": null, "legacyId": null, "subType": null, "category": null, "field2": "open", "effectiveDate": null, "objectId": "0b000064814baa40"}	single_get

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