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dockets: FDA-2026-P-10660

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-2026-P-10660 FDA Requests that the FDA take administrative actions regarding drug products containing ethinylestradiol (also known as 17α-ethinylestradiol or EE2) and combined oral contraceptives that contain ethinylestradiol. Nonrulemaking 2026-09-11T15:33:55Z 0b000064b951d315                     list_pull

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