documents: FDA-2006-N-0515-0072
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
This data as json
| 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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2006-N-0515-0072 | FDA | FDA-2006-N-0515 | Reference 3 - U.S. Food and Drug Administration, "Guidance for Industry, Warnings and Precautions, Contraindications, and Boxed Warning Sections of Labeling for Human Prescription Drug and Biological Products--Content and Format," re Content and Format of Labeling for Human Prescription Drug and Biological Products; Requirements for Pregnancy and Lactation Labeling | Supporting & Related Material | Background Material | 2014-12-05T05:00:00Z | 2014 | 12 | 2014-12-05T14:48:15Z | 0 | 0 | 090000648195b8b8 |
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- 0 rows from regs_document_id in fr_regs_crossref