documents: FDA-2014-D-0622-0020

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id agency_id docket_id title document_type subtype posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2014-D-0622-0020 FDA FDA-2014-D-0622 Best Practices in Developing Proprietary Names for Human Prescription Drug Products; Guidance for Industry; Availability Notice Notice of Availability 2020-12-09T05:00:00Z 2020 12 2020-12-09T05:00:00Z   2020-12-09T13:40:47Z 2020-27058 0 0 090000648498fb58

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