documents

Regulatory documents from Regulations.gov including rules, proposed rules, notices, and supporting materials.

Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API

48 rows where document_type = "Other" and posted_year = 2000 sorted by posted_date descending

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  • 2000 · 48 ✖

document_type 1

  • Other · 48 ✖

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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posted_date ▲ posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2000-P-0151-0001 FDA Amend definition & standard of identity for parmesan cheese-CLOSED FDA-2000-P-0151 FDA/DDM to Satori Food Corp. Other ACK-Acknowledgement Letter 2000-12-29T05:00:00Z 2000 12     2008-04-25T01:31:51Z   0 0 09000064804d117d
FDA-2000-D-0598-0002 FDA Genotoxicity Studies (VICH GL23) FDA-2000-D-0598 Guidance for Industry #116 Safety Studies for Veterinary Drug Residues in Human Food: Genotoxicity Studies VICH GL23; Draft Guidance Other Guidance 2000-12-18T05:00:00Z 2000 12 2013-01-23T05:00:00Z   2013-01-24T03:08:44Z   0 0 09000064804dd8b1
FDA-2000-P-1559-0001 FDA Action Against Manufacturers of Garlic Supplements Misbranded-CLOSED FDA-2000-P-1559 FDA/DDM to Center for Science in the Public Interest (CSPI) Other ACK-Acknowledgement Letter 2000-12-13T05:00:00Z 2000 12     2008-04-25T01:56:32Z   0 0 09000064804f9287
FDA-2000-D-0028-0002 FDA Channels trade policy commodities with methyl parathion FDA-2000-D-0028 Guidance for Industry: Channels of Trade Policy for Commodities with Methyl Parathion Residues Other Guidance 2000-11-30T05:00:00Z 2000 11 2020-09-30T04:00:00Z   2024-11-12T23:25:43Z   1 0 09000064848a2c00
FDA-1998-P-0046-0001 FDA Revoke determination that TSRH Pedicle Spinal Screw System-CLOSED FDA-1998-P-0046 FDA/CDRH to Arnold Levin Other PDN-Petition Denial 2000-11-08T05:00:00Z 2000 11     2008-05-16T21:47:38Z   0 0 090000648056e6a9
FDA-2000-P-0212-0001 FDA Remove Unapproved Children's Fluoride Supplements from Mkt FDA-2000-P-0212 New Jersey General Assembly - Citizen Petition Other CP-Citizen Petition 2000-11-06T05:00:00Z 2000 11     2010-08-12T19:47:56Z   0 0 09000064804d4d1b
FDA-2000-P-0025-0003 FDA Classify cranial helment in class I,exempt from premarket-CLOSED FDA-2000-P-0025 Petition Approval from FDA CDRH to American Orthotic & Prosthetic Association Other PAV-Petition Approval 2000-10-31T05:00:00Z 2000 10     2024-07-29T20:17:20Z   0 0 09000064804aea11
FDA-2000-P-0025-0002 FDA Classify cranial helment in class I,exempt from premarket-CLOSED FDA-2000-P-0025 Petition Approval from FDA CDRH to American Orthotic & Prosthetic Association Other PAV-Petition Approval 2000-10-31T05:00:00Z 2000 10     2024-07-29T20:14:37Z   0 0 09000064804aea10
FDA-2000-P-0153-0001 FDA ANDA Suitability Petition for Ursodiol Oral Suspension-CLOSED FDA-2000-P-0153 FDA/DDM to Lachman Consultant Services, Inc. Other ACK-Acknowledgement Letter 2000-10-16T04:00:00Z 2000 10     2008-04-25T01:45:52Z   0 0 09000064804d1408
FDA-2000-P-0096-0002 FDA Approve ANDA for Cefuroxime Axetil Products-CLOSED FDA-2000-P-0096 FDA/DDM to Arnold & Porter Other ACK-Acknowledgement Letter 2000-10-02T04:00:00Z 2000 10     2008-04-25T01:01:16Z   0 0 09000064804b8220
FDA-2000-P-0096-0001 FDA Approve ANDA for Cefuroxime Axetil Products-CLOSED FDA-2000-P-0096 FDA/DDM to Arnold & Porter Other ACK-Acknowledgement Letter 2000-10-02T04:00:00Z 2000 10     2008-04-25T01:01:17Z   0 0 09000064804b8209
FDA-2000-P-0214-0001 FDA ANDA for Sertraline Hydrochloride Capsules 25mg, 50mg & 100m-CLOSED FDA-2000-P-0214 FDA/DDM to Lachman Consultant Services, Inc. Other ACK-Acknowledgement Letter 2000-08-22T04:00:00Z 2000 8     2008-04-25T01:14:23Z   0 0 09000064804d4e50
FDA-2000-P-0211-0003 FDA Amend the Product Insert and/or Label for Anthrax Vaccine Adsorbed FDA-2000-P-0211 FDA/CBER to Mark S. Zaid Other LET-Letter 2000-08-16T04:00:00Z 2000 8     2008-04-25T01:47:40Z   0 0 09000064804d4cd2
FDA-2000-P-0211-0002 FDA Amend the Product Insert and/or Label for Anthrax Vaccine Adsorbed FDA-2000-P-0211 FDA/CBER to Mark S. Zaid Other LET-Letter 2000-08-16T04:00:00Z 2000 8     2008-04-25T01:47:40Z   0 0 09000064804d4cd0
FDA-1980-N-0074-0071 FDA Anticaries Drug Products for OTC Human Use; FDA-1980-N-0074 HFD-560 Other MM-Memorandum of Meeting 2000-08-09T04:00:00Z 2000 8     2008-05-30T22:52:54Z   0 0 09000064805bb4d0
FDA-1978-N-0018-0439 FDA Sunscreen Drug Products -OPEN FDA-1978-N-0018 Memorandum of Meeting Between FDA/CDER and External Participants Other Memorandum 2000-08-07T04:00:00Z 2000 8     2019-08-06T19:13:07Z   0 0 090000648055a6cc
FDA-1978-N-0018-0438 FDA Sunscreen Drug Products -OPEN FDA-1978-N-0018 Memorandum of Meeting Between FDA/CDER Participants and External Participants Other Memorandum 2000-08-07T04:00:00Z 2000 8     2019-08-06T18:35:41Z   0 0 090000648055a6c9
FDA-2020-D-1956-0001 FDA FDA-2020-D-1956 Guidance for Industry: Action Levels for Poisonous or Deleterious Substances in Human Food and Animal Feed Other Guidance 2000-07-31T04:00:00Z 2000 7 2020-09-21T04:00:00Z   2024-11-12T23:24:59Z   1 0 090000648486938e
FDA-2000-P-0024-0002 FDA ANDA Suitability for Hydrocodone Bitartrate/Acetaminophen-CLOSED FDA-2000-P-0024 FDA/DDM to Pharmaceutical Associates, Inc Other ACK-Acknowledgement Letter 2000-07-26T04:00:00Z 2000 7     2008-04-25T01:13:49Z   0 0 09000064804ae9ff
FDA-1999-H-0116-0001 FDA Civil Money Penalties;Westfield Food Mart Inc,d/b/a Shell FDA-1999-H-0116 Office of Tobacco Programs Other LET-Letter 2000-07-18T04:00:00Z 2000 7     2009-07-07T18:08:47Z   0 0 09000064804ae912
FDA-1999-H-0143-0001 FDA Civil Money Penalties; Triple V Inc,d/b/a Country Market FDA-1999-H-0143 Office of Tobacco Programs Other LET-Letter 2000-07-18T04:00:00Z 2000 7     2009-07-07T18:13:38Z   0 0 09000064804aef05
FDA-1999-H-0018-0001 FDA Civil Money Penalties; Carlie C's IGA Inc FDA-1999-H-0018 Office of Tobacco Programs Other LET-Letter 2000-07-12T04:00:00Z 2000 7     2009-07-07T14:12:12Z   0 0 09000064804a5a99
FDA-1999-H-0017-0001 FDA Civil Money Penalties;R.G. Stocks & Son, Inc,d/b/a Stocks FDA-1999-H-0017 Office of Tobacco Programs Other LET-Letter 2000-07-12T04:00:00Z 2000 7     2009-07-07T13:29:31Z   0 0 09000064804a5a88
FDA-1999-H-0017-0002 FDA Civil Money Penalties;R.G. Stocks & Son, Inc,d/b/a Stocks FDA-1999-H-0017 FDA/CDRH/GCF Other CR-Correction 2000-07-12T04:00:00Z 2000 7     2009-07-07T14:01:38Z   0 0 09000064804a5a91
FDA-1999-H-0054-0001 FDA Civil Money Penalties;Eckerd Corp,d/b/a Eckerd Drug #8608 FDA-1999-H-0054 Office of Tobacco Programs Other LET-Letter 2000-07-07T04:00:00Z 2000 7     2009-07-07T14:13:40Z   0 0 09000064804a61a3
FDA-1980-N-0074-0070 FDA Anticaries Drug Products for OTC Human Use; FDA-1980-N-0074 HFD-560 Other MM-Memorandum of Meeting 2000-06-28T04:00:00Z 2000 6     2008-05-30T22:53:02Z   0 0 09000064805bb4cf
FDA-1999-H-0071-0001 FDA Civil Money Penalty; Dong Seo Shin d/b/a East 4th Avenue Food Mart FDA-1999-H-0071 HHS/FDA/CDER Notice of Correction of Store Name - Correction Other CR-Correction 2000-06-15T04:00:00Z 2000 6     2013-07-27T20:58:49Z   0 0 09000064804a6880
FDA-1995-S-0039-0320 FDA 75-Day Premarket Notifications for New Dietary Ingredients FDA-1995-S-0039 Report from FDA/CFSAN Other Report 2000-05-21T04:00:00Z 2000 5 2014-02-28T05:00:00Z   2016-09-30T14:25:01Z   0 0 090000648055c40f
FDA-1980-N-0074-0069 FDA Anticaries Drug Products for OTC Human Use; FDA-1980-N-0074 HFD-560, CDER HFD-105 and Warner Lambert Other MM-Memorandum of Meeting 2000-04-27T04:00:00Z 2000 4     2008-05-30T22:52:47Z   0 0 09000064805bb4c7
FDA-1995-S-0039-0169 FDA 75-Day Premarket Notifications for New Dietary Ingredients FDA-1995-S-0039 Report from FDA/CFSAN Other RPT-Report (outside of agency unless indicated) 2000-04-19T04:00:00Z 2000 4 2009-02-05T05:00:00Z   2016-09-30T14:23:12Z   0 0 090000648055c40d
FDA-1995-S-0039-0168 FDA 75-Day Premarket Notifications for New Dietary Ingredients FDA-1995-S-0039 Report from FDA/CFSAN Other RPT-Report (outside of agency unless indicated) 2000-04-18T04:00:00Z 2000 4 2009-02-05T05:00:00Z   2016-09-30T14:23:11Z   0 0 090000648055c40b
FDA-1980-P-0012-0014 FDA Showlasers model LP1-CLOSED FDA-1980-P-0012 Approval for Variance from FDA/CDRH to Showlasers, Inc. (duplicate) Other Approval for Variance (VRA) 2000-04-13T04:00:00Z 2000 4     2021-02-24T17:53:01Z   0 0 09000064805b926d
FDA-1980-P-0012-0013 FDA Showlasers model LP1-CLOSED FDA-1980-P-0012 Approval for Variance from FDA/CDRH to Showlasers, Inc. Other Approval for Variance (VRA) 2000-04-13T04:00:00Z 2000 4     2021-02-24T17:51:26Z   0 0 09000064805b926c
FDA-2000-P-0024-0001 FDA ANDA Suitability for Hydrocodone Bitartrate/Acetaminophen-CLOSED FDA-2000-P-0024 FDA/DDM to Pharmaceutical Associates Inc Other ACK-Acknowledgement Letter 2000-04-07T04:00:00Z 2000 4     2008-04-25T01:13:49Z   0 0 09000064804ae9e8
FDA-1999-P-0126-0006 FDA Abbreviated new drug application/topical dematological drug-CLOSED FDA-1999-P-0126 FDA/CDER to Pharmacia & Upjohn Other LET-Letter 2000-04-06T04:00:00Z 2000 4     2008-04-25T00:19:51Z   0 0 09000064804ae9f2
FDA-1999-P-0059-0002 FDA Reg/Guide to Label Medical Devices contain'g Phthalate Plasticizers-CLOSED FDA-1999-P-0059 FDA/CDRH to Sanford J. Lewis Other LET-Letter 2000-04-06T04:00:00Z 2000 4     2008-04-25T00:13:57Z   0 0 09000064804a6715
FDA-1986-V-0022-0009 FDA Ion laser technology series ILT 5000 Demo unit FDA-1986-V-0022 Variance Approval Letter from FDA CDRH to California Technical Associates Other Approval for Variance (VRA) 2000-03-22T05:00:00Z 2000 3     2023-01-18T18:47:01Z   0 0 090000648050dd45
FDA-1991-V-0023-0005 FDA Las Vegas laser rental light shows. FDA-1991-V-0023 Variance Approval Letter from FDA CDRH to Las Vegas Laser Rental Other Approval for Variance (VRA) 2000-03-22T05:00:00Z 2000 3     2023-10-13T12:19:38Z   0 0 0900006480528680
FDA-2000-P-0025-0001 FDA Classify cranial helment in class I,exempt from premarket-CLOSED FDA-2000-P-0025 Acknowledgment Letter from FDA DMB to American Orthotic & Prosthetic Association Other ACK-Acknowledgement Letter 2000-03-14T05:00:00Z 2000 3     2024-07-29T20:12:00Z   0 0 09000064804aea0c
FDA-2000-D-1542-0002 FDA Content/Format of NDA/ANDA for Certain Positron Emission FDA-2000-D-1542 Draft Guidance for Industry on the Content and Format of New Drug Applications and Abbreviated New Drug Applications for Certain Positron Emission Tomography Drug Products - Guidance Other GDL-Guidance (Supporting and Related Materials) 2000-03-10T19:46:00Z 2000 3 2000-03-10T05:00:00Z   2019-10-17T17:11:55Z   0 0 09000064804f9073
FDA-1995-S-0039-0167 FDA 75-Day Premarket Notifications for New Dietary Ingredients FDA-1995-S-0039 Report from FDA/CFSAN Other RPT-Report (outside of agency unless indicated) 2000-02-17T05:00:00Z 2000 2 2009-02-05T05:00:00Z   2016-09-30T14:23:11Z   0 0 090000648055c402
FDA-1995-S-0039-0166 FDA 75-Day Premarket Notifications for New Dietary Ingredients FDA-1995-S-0039 Report from FDA/CFSAN Other RPT-Report (outside of agency unless indicated) 2000-02-17T05:00:00Z 2000 2 2009-02-05T05:00:00Z   2016-09-30T14:23:11Z   0 0 090000648055c3fe
FDA-2000-P-0211-0001 FDA Amend the Product Insert and/or Label for Anthrax Vaccine Adsorbed FDA-2000-P-0211 FDA/DDM to Mark S. Zaid Other ACK-Acknowledgement Letter 2000-02-16T05:00:00Z 2000 2     2008-04-25T01:47:40Z   0 0 09000064804d4c9f
FDA-1998-P-0018-0003 FDA Drug products containing oxycodone hydrocloride tablet suitable-CLOSED FDA-1998-P-0018 Correction to Citizen Petition from King & Spalding Other Correction(s) 2000-02-14T05:00:00Z 2000 2     2024-07-12T16:52:34Z   0 0 0900006480563c52
FDA-1999-D-0061-0003 FDA Testing Orthopedic Implants with Metallic Plasma Sprayed FDA-1999-D-0061 HFZ-220 Other NAD-Notice of Availability of Data 2000-02-03T05:00:00Z 2000 2     2024-11-07T21:52:50Z   1 0 09000064804a6774
FDA-1996-N-0006-0003 FDA Eligibility Criteria for Considering Additional Conditions in the Over-the-Counter Drug Monograph System FDA-1996-N-0006 Memorandum of Meeting FDA with European Sunscreen Manufacturers re Sunscreen Monograph/Foreign Marketing October 28, 1998 Other Memorandum 2000-01-20T05:00:00Z 2000 1     2015-03-20T16:01:26Z   0 0 09000064804f9943
FDA-2020-D-1957-0001 FDA FDA-2020-D-1957 CPG Sec. 300.200 - Reconditioners/Rebuilders of Medical Devices - Revoked-Deletion 01/04/2000 Other Guidance 2000-01-03T05:00:00Z 2000 1 2020-09-21T04:00:00Z   2024-11-06T23:39:28Z   1 0 0900006484869390
FDA-1995-S-0039-0157 FDA 75-Day Premarket Notifications for New Dietary Ingredients FDA-1995-S-0039 Report from FDA/CFSAN Other RPT-Report (outside of agency unless indicated) 2000-01-01T05:00:00Z 2000 1 2009-01-02T05:00:00Z   2016-09-30T14:23:07Z   0 0 090000648055c3f8

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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);