dockets: FDA-2005-P-0319

Regulatory dockets from Regulations.gov — containers for related documents and comments in a rulemaking proceeding.

This data as json

id	agency_id	title	docket_type	last_modified	object_id
FDA-2005-P-0319	FDA	Withhold Approval of any ANDA or any 505(b)(2) Application for any Generic Version or Other Pharmaceutical Alternative of Venofer(Iron Sucrose Injection, USP)	Nonrulemaking	2025-08-08T15:50:15Z	0b00006480447df4

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