dockets: FDA-2008-P-0662

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-2008-P-0662	FDA	ANDA Suitability for Rifampkin Oral Suspension, 50 mg/5 mL and 10 mg/5 mL	Nonrulemaking	2022-01-05T01:03:34Z	0b0000648080800b					["ANDA Suitability ", "Rifampkin Oral Suspension", "50 mg/5 mL ", "10 mg/5 mL", "CDER"]	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."}], "keywords": ["ANDA Suitability ", "Rifampkin Oral Suspension", "50 mg/5 mL ", "10 mg/5 mL", "CDER"], "modifyDate": "2022-01-05T01:03:34Z", "dkAbstract": null, "agencyId": "FDA", "program": "CDER", "shortTitle": null, "subType2": null, "title": "ANDA Suitability for Rifampkin Oral Suspension, 50 mg/5 mL and 10 mg/5 mL", "generic": "P", "field1": null, "docketType": "Nonrulemaking", "petitionNbr": null, "rin": null, "organization": null, "legacyId": null, "subType": null, "category": null, "field2": null, "effectiveDate": null, "objectId": "0b0000648080800b"}	single_get

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