documents: FDA-2020-D-0770-0001

Regulatory documents from Regulations.gov including rules, proposed rules, notices, and supporting materials.

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2020-D-0770-0001 FDA FDA-2020-D-0770 Best Practices in Developing Proprietary Names for Human Nonprescription Drug Products; Draft Guidance for Industry; Availability Notice Notice of Availability 2020-12-09T05:00:00Z 2020 12 2020-12-09T05:00:00Z   2021-03-15T21:11:29Z 2020-27057 0 0 090000648498fbf4

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