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documents: FDA-2020-D-0770-0002

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-0770-0002 FDA FDA-2020-D-0770 Best Practices in Developing Proprietary Names for Non-Prescription Drug Products; Guidance for Industry; Draft Guidance Other Guidance 2020-12-09T05:00:00Z 2020 12 2020-12-09T05:00:00Z 2021-02-09T04:59:59Z 2024-11-06T23:43:04Z   1 0 090000648498f748

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