documents
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
12 rows where docket_id = "FDA-1993-N-0043" sorted by posted_date descending
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Suggested facets: title, subtype, posted_date, posted_month, comment_start_date, comment_end_date, last_modified, posted_date (date), comment_start_date (date), comment_end_date (date), last_modified (date)
document_type 2
agency_id 1
- FDA 12
| 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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-1993-N-0043-0007 | FDA | Adverse Experience Reporting Requirements Drug/Biologicals FDA-1993-N-0043 | Expedited Safety Reporting Requirements for Human Drug and Biological Products; Correction | Notice | Correction | 1998-03-26T05:00:00Z | 1998 | 3 | 2024-04-29T15:00:31Z | 0 | 0 | 09000064804fc45a | |||
| FDA-1993-N-0043-0005 | FDA | Adverse Experience Reporting Requirements Drug/Biologicals FDA-1993-N-0043 | (COPY)- Expedited Safety Reporting Requirements for Human Drug and Biological Products | Notice | Notice of Final Rule | 1997-10-09T04:00:00Z | 1997 | 10 | 1997-10-09T04:00:00Z | 1997-12-09T04:59:59Z | 2024-04-29T15:09:23Z | 0 | 0 | 09000064804fc456 | |
| FDA-1993-N-0043-0006 | FDA | Adverse Experience Reporting Requirements Drug/Biologicals FDA-1993-N-0043 | (COPY)- Expedited Safety Reporting Requirements for Human Drug and Biological Products | Notice | Notice of Final Rule | 1997-10-09T04:00:00Z | 1997 | 10 | 1997-10-09T04:00:00Z | 1997-12-09T04:59:59Z | 2024-04-29T15:10:12Z | 0 | 0 | 09000064804fc457 | |
| FDA-1993-N-0043-0004 | FDA | Adverse Experience Reporting Requirements Drug/Biologicals FDA-1993-N-0043 | Expedited Safety Reporting Requirements for Human Drug and Biological Products | Notice | Notice of Final Rule | 1997-10-09T04:00:00Z | 1997 | 10 | 1997-10-09T04:00:00Z | 1997-12-09T04:59:59Z | 2024-04-29T15:08:44Z | 0 | 0 | 09000064804fc455 | |
| FDA-1993-N-0043-0003 | FDA | Adverse Experience Reporting Requirements Drug/Biologicals FDA-1993-N-0043 | Adverse Experience Reporting Requirements for Human Drug, Correction | Notice | Correction | 1995-01-24T05:00:00Z | 1995 | 1 | 2024-04-29T14:55:05Z | 0 | 0 | 09000064804fc3ce | |||
| FDA-1993-N-0043-0002 | FDA | Adverse Experience Reporting Requirements Drug/Biologicals FDA-1993-N-0043 | Adverse Experience Reporting Requirements for Human Drug and Licensed Biological Products; Correction | Notice | Correction | 1994-12-05T05:00:00Z | 1994 | 12 | 2024-04-29T14:48:41Z | 0 | 0 | 09000064804fc3bb | |||
| FDA-1993-N-0043-0001 | FDA | Adverse Experience Reporting Requirements Drug/Biologicals FDA-1993-N-0043 | Adverse Experience Reporting Requirements for Human Drug and Licensed Biological Products | Notice | NPR-Notice of Proposed Rule-Making | 1994-11-15T05:00:00Z | 1994 | 11 | 1994-11-15T05:00:00Z | 1995-01-26T04:59:59Z | 2024-04-29T14:42:48Z | 0 | 0 | 09000064804fc3b4 | |
| FDA-1993-N-0043-0009 | FDA | Adverse Experience Reporting Requirements Drug/Biologicals FDA-1993-N-0043 | Background Material | Supporting & Related Material | BKG-Background Material | 1994-10-26T04:00:00Z | 1994 | 10 | 2008-05-16T23:24:08Z | 0 | 0 | 09000064804fc45c | |||
| FDA-1993-N-0043-0011 | FDA | Adverse Experience Reporting Requirements Drug/Biologicals FDA-1993-N-0043 | Background Material | Supporting & Related Material | BKG-Background Material | 1994-10-26T04:00:00Z | 1994 | 10 | 2008-05-16T23:24:08Z | 0 | 0 | 09000064804fc45e | |||
| FDA-1993-N-0043-0008 | FDA | Adverse Experience Reporting Requirements Drug/Biologicals FDA-1993-N-0043 | Background Material | Supporting & Related Material | BKG-Background Material | 1994-10-26T04:00:00Z | 1994 | 10 | 2008-05-16T23:24:10Z | 0 | 0 | 09000064804fc45b | |||
| FDA-1993-N-0043-0012 | FDA | Adverse Experience Reporting Requirements Drug/Biologicals FDA-1993-N-0043 | Background Material | Supporting & Related Material | BKG-Background Material | 1994-10-26T04:00:00Z | 1994 | 10 | 2008-05-16T23:24:10Z | 0 | 0 | 09000064804fc45f | |||
| FDA-1993-N-0043-0010 | FDA | Adverse Experience Reporting Requirements Drug/Biologicals FDA-1993-N-0043 | Background Material | Supporting & Related Material | BKG-Background Material | 1994-10-26T04:00:00Z | 1994 | 10 | 2008-05-16T23:24:09Z | 0 | 0 | 09000064804fc45d |
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CREATE TABLE documents (
id TEXT PRIMARY KEY,
agency_id TEXT,
docket_id TEXT REFERENCES dockets(id),
title TEXT,
document_type TEXT,
subtype TEXT,
posted_date TEXT,
posted_year INTEGER,
posted_month INTEGER,
comment_start_date TEXT,
comment_end_date TEXT,
last_modified TEXT,
fr_doc_num TEXT,
open_for_comment INTEGER,
withdrawn INTEGER,
object_id TEXT
);
CREATE INDEX idx_docs_agency ON documents(agency_id);
CREATE INDEX idx_docs_docket ON documents(docket_id);
CREATE INDEX idx_docs_date ON documents(posted_date);
CREATE INDEX idx_docs_year ON documents(posted_year);
CREATE INDEX idx_docs_type ON documents(document_type);
CREATE INDEX idx_docs_frnum ON documents(fr_doc_num);