dockets: FDA-2026-P-5017

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
FDA-2026-P-5017	FDA	Request that the FDA determine whether the Reference Listed Drug (RLD) VELTASSA (PATIROMER SORBITEX CALCIUM) Oral Powder, Eq 25.2 gm Base/Packet; under New Drug Application (NDA) 205739 held by VIFOR PHARMA INC, was voluntarily withdrawn from commercial distribution, or withdrawn from sale for safety or efficacy reasons	Nonrulemaking	2026-05-07T19:44:54Z	0b000064b92c7bf5

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