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Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
66 rows where document_type = "Other" and posted_year = 1995 sorted by posted_date descending
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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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-1978-N-2157-0006 | FDA | Skin Protectant Drug Proposed Rulemaking for Diaper Rash FDA-1978-N-2157 | Acknowledgement Letter FDA/DDM to The Proctor & Gamble Company | Other | Acknowledgement Letter/Receipt | 1995-12-22T05:00:00Z | 1995 | 12 | 2019-08-01T18:37:54Z | 0 | 0 | 09000064805a6715 | |||
| FDA-1978-N-2157-0004 | FDA | Skin Protectant Drug Proposed Rulemaking for Diaper Rash FDA-1978-N-2157 | Acknowledgement Letter FDA/DDM to Huls America, Inc. | Other | Acknowledgement Letter/Receipt | 1995-12-22T05:00:00Z | 1995 | 12 | 2019-08-01T18:45:05Z | 0 | 0 | 09000064805a6713 | |||
| FDA-1978-N-2157-0005 | FDA | Skin Protectant Drug Proposed Rulemaking for Diaper Rash FDA-1978-N-2157 | Acknowledgment Letter from FDA/DDM to Smith & Nephew United Inc. re: Citizen Petition from Smith & Nephew United, Inc. | Other | Acknowledgement Letter/Receipt | 1995-12-22T05:00:00Z | 1995 | 12 | 2019-06-03T13:50:38Z | 0 | 0 | 09000064805a6714 | |||
| FDA-1995-P-0044-0003 | FDA | Modify Advice Bioequivalence of generic ammonium lactate-CLOSED FDA-1995-P-0044 | FDA/DDM to Westwood Squibb Pharmaceuticals, Inc | Other | ACK-Acknowledgement Letter | 1995-11-27T05:00:00Z | 1995 | 11 | 2008-05-16T23:07:30Z | 0 | 0 | 090000648056143f | |||
| FDA-1978-N-0018-0144 | FDA | Sunscreen Drug Products -OPEN FDA-1978-N-0018 | Letter from The Assembly State of New York, Albany to FDA | Other | Letter(s) | 1995-11-22T05:00:00Z | 1995 | 11 | 2019-07-23T18:14:02Z | 0 | 0 | 090000648055a251 | |||
| FDA-1995-P-0023-0001 | FDA | Add Terminal Dry-Heat Inactivation of Plasma-Derived Factor8-CLOSED FDA-1995-P-0023 | HFA-305 to Columbia University of School of Public Health | Other | ACK-Acknowledgement Letter | 1995-11-20T05:00:00Z | 1995 | 11 | 2008-05-16T23:07:11Z | 0 | 0 | 0900006480559662 | |||
| FDA-1995-P-0010-0001 | FDA | Current Good Manufacturing Practices Regulations for Medicated Feeds FDA-1995-P-0010 | Acknowledgement Letter to American Feed Industry Association and Animal Health Institute | Other | ACK-Acknowledgement Letter | 1995-11-14T05:00:00Z | 1995 | 11 | 2013-07-28T01:44:10Z | 0 | 0 | 090000648055842e | |||
| FDA-1978-N-0018-0143 | FDA | Sunscreen Drug Products -OPEN FDA-1978-N-0018 | Memorandum of Meeting Between FDA and Givaudan-Roure Corporation et al August 11, 1995 | Other | Memorandum | 1995-11-01T05:00:00Z | 1995 | 11 | 2019-07-23T16:14:40Z | 0 | 0 | 090000648055a248 | |||
| FDA-1995-P-0042-0001 | FDA | Regulate Caffeine Beverages as Drugs and/or Devices-CLOSED FDA-1995-P-0042 | Acknowledgment Letter from FDA DMB to Competitive Enterprise Institute | Other | ACK-Acknowledgement Letter | 1995-10-31T05:00:00Z | 1995 | 10 | 2025-09-15T16:26:01Z | 0 | 0 | 090000648056126b | |||
| FDA-1982-P-0001-0011 | FDA | Bacitracin Zinc Premix FDA-1982-P-0001 | FDA/Associate Commissioner for Regulatory Affairs | Other | PDN-Petition Denial | 1995-10-27T04:00:00Z | 1995 | 10 | 2008-05-30T22:53:10Z | 0 | 0 | 090000648050d497 | |||
| FDA-1978-N-0018-0142 | FDA | Sunscreen Drug Products -OPEN FDA-1978-N-0018 | Letter from FDA CDER to the Honorable Audrey I. Pheffer & Harvey Weisenberg, New York State Assembly | Other | Letter(s) | 1995-10-26T04:00:00Z | 1995 | 10 | 2019-07-23T16:02:30Z | 0 | 0 | 090000648055a246 | |||
| FDA-1995-P-0004-0001 | FDA | ANDA Suitability for 2.5mg Hydrocodone Bitrate & 5mg Phenylephrine-CLOSED FDA-1995-P-0004 | Acknowledgement Letter from FDA DMB to Bock Pharmacal Co | Other | Acknowledgement Letter/Receipt | 1995-10-12T04:00:00Z | 1995 | 10 | 2024-06-06T01:00:29Z | 0 | 0 | 09000064805583cb | |||
| FDA-1980-N-0074-0032 | FDA | Anticaries Drug Products for OTC Human Use; FDA-1980-N-0074 | Letter from FDA HFD-811 to Cosmetic, Toiletry and Fragrance Association | Other | Letter(s) | 1995-10-04T04:00:00Z | 1995 | 10 | 2022-04-21T20:23:50Z | 0 | 0 | 09000064805bb362 | |||
| FDA-1995-S-0039-0001 | FDA | 75-Day Premarket Notifications for New Dietary Ingredients FDA-1995-S-0039 | Memorandum from FDA/CFSAN | Other | M-Memorandum | 1995-09-27T04:00:00Z | 1995 | 9 | 2016-09-30T14:17:47Z | 0 | 0 | 090000648055bacf | |||
| FDA-1991-P-0020-0001 | FDA | Ban the Advertising of Prescription Drugs - CLOSED FDA-1991-P-0020 | Letter from FDA to Bass & Ullman on Behalf of National Association of Pharmaceutical Manufacturers | Other | Letter(s) | 1995-08-28T04:00:00Z | 1995 | 8 | 2023-11-16T21:52:45Z | 0 | 0 | 09000064805284a2 | |||
| FDA-1995-P-0006-0003 | FDA | ANDA for Butalbital, Acetaminophen, Caffeine and Hydrocodone-CLOSED FDA-1995-P-0006 | Acknowledgment Letter from FDA DMB to Mikart, Inc. | Other | Acknowledgement Letter/Receipt | 1995-08-21T04:00:00Z | 1995 | 8 | 2025-09-19T00:46:55Z | 0 | 0 | 0900006480558400 | |||
| FDA-1995-P-0006-0002 | FDA | ANDA for Butalbital, Acetaminophen, Caffeine and Hydrocodone-CLOSED FDA-1995-P-0006 | Acknowledgment Letter from FDA DMB to Mikart, Inc. | Other | Acknowledgement Letter/Receipt | 1995-08-21T04:00:00Z | 1995 | 8 | 2025-09-19T00:46:31Z | 0 | 0 | 09000064805583ff | |||
| FDA-1995-P-0006-0004 | FDA | ANDA for Butalbital, Acetaminophen, Caffeine and Hydrocodone-CLOSED FDA-1995-P-0006 | Acknowledgment Letter from FDA DMB to Mikart, Inc. | Other | Acknowledgement Letter/Receipt | 1995-08-21T04:00:00Z | 1995 | 8 | 2025-09-19T00:47:17Z | 0 | 0 | 0900006480558401 | |||
| FDA-1995-P-0006-0001 | FDA | ANDA for Butalbital, Acetaminophen, Caffeine and Hydrocodone-CLOSED FDA-1995-P-0006 | Acknowledgment Letter from FDA DMB to Mikart, Inc. | Other | Acknowledgement Letter/Receipt | 1995-08-18T04:00:00Z | 1995 | 8 | 2025-09-19T00:45:55Z | 0 | 0 | 09000064805583f5 | |||
| FDA-1995-P-0002-0002 | FDA | Revise "Approved Drug Products" (known as "Orange Book")-CLOSED FDA-1995-P-0002 | HFA-305 to Kleinfeld, Kaplan & Becker | Other | ACK-Acknowledgement Letter | 1995-08-11T04:00:00Z | 1995 | 8 | 2008-05-16T23:06:15Z | 0 | 0 | 0900006480558353 | |||
| FDA-1995-P-0360-0002 | FDA | Regulatory Action to Prohibit Misleading Food Labeling FDA-1995-P-0360 | Acknowledgement Letter to Citizen Petition from Center for Science in the Public Interest | Other | Acknowledgement Letter/Receipt | 1995-08-04T04:00:00Z | 1995 | 8 | 2015-04-05T04:00:00Z | 2015-04-05T13:56:53Z | 0 | 0 | 0900006481a8be2c | ||
| FDA-1995-P-0360-0001 | FDA | Regulatory Action to Prohibit Misleading Food Labeling FDA-1995-P-0360 | Citizen Petition from Center for Science in the Public Interest | Other | Citizen Petition | 1995-08-04T04:00:00Z | 1995 | 8 | 2015-04-05T04:00:00Z | 2015-04-05T13:57:11Z | 0 | 0 | 090000648059a009 | ||
| FDA-1995-P-0016-0003 | FDA | Implied Nutrient Content Claim 'Healthy' & Health Claims-CLOSED FDA-1995-P-0016 | HFA-305 | Other | ACK-Acknowledgement Letter | 1995-07-28T04:00:00Z | 1995 | 7 | 2008-05-16T23:06:36Z | 0 | 0 | 0900006480558657 | |||
| FDA-1988-V-0025-0001 | FDA | Variance re Laser light show projector (LIP-88-1) FDA-1988-V-0025 | Approval for Variance from Laser Images Productions | Other | Approval for Variance (VRA) | 1995-07-20T04:00:00Z | 1995 | 7 | 2023-12-01T16:06:11Z | 0 | 0 | 09000064804763b9 | |||
| FDA-1995-P-0018-0002 | FDA | ANDA Suit for Hydrocodone Bitartrate & Acetaminophen-CLOSED FDA-1995-P-0018 | Acknowledgment Letter from FDA DMB to Mikart, Inc. | Other | Acknowledgement Letter/Receipt | 1995-07-20T04:00:00Z | 1995 | 7 | 2025-07-07T17:49:13Z | 0 | 0 | 09000064805592aa | |||
| FDA-1995-P-0018-0001 | FDA | ANDA Suit for Hydrocodone Bitartrate & Acetaminophen-CLOSED FDA-1995-P-0018 | Acknowledgment Letter from FDA DMB to Mikart, Inc. | Other | Acknowledgement Letter/Receipt | 1995-07-20T04:00:00Z | 1995 | 7 | 2025-10-11T08:00:48Z | 0 | 0 | 0900006480559274 | |||
| FDA-1978-N-0018-0141 | FDA | Sunscreen Drug Products -OPEN FDA-1978-N-0018 | Letter from FDA CDER to Paul Pierce | Other | Letter(s) | 1995-07-13T04:00:00Z | 1995 | 7 | 2019-07-31T14:03:30Z | 0 | 0 | 090000648055a240 | |||
| FDA-1995-P-0017-0001 | FDA | Oat Products and Coronary Heart Disease FDA-1995-P-0017 | HFS-150 to The Quaker Oats Company | Other | ACK-Acknowledgement Letter | 1995-07-06T04:00:00Z | 1995 | 7 | 2008-05-16T23:06:49Z | 0 | 0 | 0900006480558802 | |||
| FDA-1995-P-0041-0001 | FDA | Exempt Medical Gases from the Requirements of 21 CFR 205-CLOSED FDA-1995-P-0041 | Acknowledgment Letter from FDA DDM to Compressed Gas Association, Inc. | Other | Acknowledgement Letter/Receipt | 1995-06-26T04:00:00Z | 1995 | 6 | 2017-02-14T15:24:15Z | 0 | 0 | 09000064805611af | |||
| FDA-1995-P-0051-0004 | FDA | Ban the Use of Lindane as a Treatment for Lice and Scabies-CLOSED FDA-1995-P-0051 | Acknowledgment Letter from FDA DMB to Public Citzen Health Research Group | Other | Acknowledgement Letter/Receipt | 1995-06-16T04:00:00Z | 1995 | 6 | 2025-09-15T21:41:17Z | 0 | 0 | 0900006480561e5c | |||
| FDA-2020-D-2006-0001 | FDA | FDA-2020-D-2006 | Guidance for Industry: Letter to Manufacturers, Importers, and Distributors of Imported Candy and Candy Wrappers | Other | Guidance | 1995-06-13T04:00:00Z | 1995 | 6 | 2020-09-23T04:00:00Z | 2024-11-06T23:39:05Z | 1 | 0 | 09000064848746a5 | ||
| FDA-1995-P-0058-0001 | FDA | Enforce SMDA & Existing Regs Re: Mfgs of dental lubricants-CLOSED FDA-1995-P-0058 | Acknowledgment Letter from FDA DMB to Lerch, McDaniel & Kauo, PLC | Other | Acknowledgement Letter/Receipt | 1995-06-06T04:00:00Z | 1995 | 6 | 2025-09-09T09:00:16Z | 0 | 0 | 090000648056c3d3 | |||
| FDA-1995-P-0015-0001 | FDA | Amend Monograph on Antiemetic Drug Prods for OTC Human Use-CLOSED FDA-1995-P-0015 | Acknowledgement Letter from FDA HFA-305 to Akin, Grump, Strauss, Hauer & Feld, L.L.P | Other | Acknowledgement Letter/Receipt | 1995-05-30T04:00:00Z | 1995 | 5 | 2022-08-17T18:52:38Z | 0 | 0 | 0900006480558564 | |||
| FDA-1978-N-0018-0140 | FDA | Sunscreen Drug Products -OPEN FDA-1978-N-0018 | Memorandum of Telephone Conversation Between Dr. Weinstock, Brown University & Jeanne Rippere, FDA April 18, 1995 | Other | Memorandum | 1995-05-11T04:00:00Z | 1995 | 5 | 2019-07-31T14:07:58Z | 0 | 0 | 090000648055a230 | |||
| FDA-1978-N-0018-0139 | FDA | Sunscreen Drug Products -OPEN FDA-1978-N-0018 | Memorandum of Telephone Conversation Between Dr. J. Ferguson, Boots Contract Manufacturing & Jeanne Rippere, FDA May 1, 1995 | Other | Memorandum | 1995-05-11T04:00:00Z | 1995 | 5 | 2019-07-23T13:31:51Z | 0 | 0 | 090000648055a22d | |||
| FDA-1994-P-0013-0002 | FDA | Reference Amount of Wild Rice-CLOSED FDA-1994-P-0013 | Letter from FDA CFSAN to Minnesota Cultivated Wild Rice Council- Envelope | Other | Letter(s) | 1995-04-24T04:00:00Z | 1995 | 4 | 2024-06-27T03:31:05Z | 0 | 0 | 09000064804fc7db | |||
| FDA-1995-P-0043-0001 | FDA | Prescription Drug Advertisements-CLOSED FDA-1995-P-0043 | Acknowledgement Letter to Sonnenreich, Roccograndi & Woo | Other | Acknowledgement Letter/Receipt | 1995-04-24T04:00:00Z | 1995 | 4 | 2012-09-20T17:09:08Z | 0 | 0 | 090000648056133f | |||
| FDA-1994-P-0013-0001 | FDA | Reference Amount of Wild Rice-CLOSED FDA-1994-P-0013 | Letter from FDA CFSAN to Minnesota Cultivated Wild Rice Council | Other | Letter(s) | 1995-04-24T04:00:00Z | 1995 | 4 | 2024-06-27T03:29:24Z | 0 | 0 | 09000064804fc7a4 | |||
| FDA-1981-N-0013-0012 | FDA | Oral Health Care Drug Products for OTC Human Use FDA-1981-N-0013 | HFA-305 to SmithKline Beecham Consumer Healthcare | Other | ACK-Acknowledgement Letter | 1995-04-14T04:00:00Z | 1995 | 4 | 2008-05-30T22:52:38Z | 0 | 0 | 09000064805aec25 | |||
| FDA-1995-P-0035-0002 | FDA | Use URAA to Determine Approval eff date of ANDA's-CLOSED FDA-1995-P-0035 | HFA-305 to Arnold & Porter | Other | ACK-Acknowledgement Letter | 1995-03-31T05:00:00Z | 1995 | 3 | 2008-05-16T23:07:26Z | 0 | 0 | 090000648055af3a | |||
| FDA-1981-N-0013-0013 | FDA | Oral Health Care Drug Products for OTC Human Use FDA-1981-N-0013 | HFA-305 to SmithKline Beecham Consumer Healthcare | Other | ACK-Acknowledgement Letter | 1995-03-29T05:00:00Z | 1995 | 3 | 2008-05-30T22:53:17Z | 0 | 0 | 09000064805aec26 | |||
| FDA-1978-N-0018-0138 | FDA | Sunscreen Drug Products -OPEN FDA-1978-N-0018 | Memorandum of Meeting Between FDA and Givaudan-Roure, et al. March 6, 1995 | Other | Memorandum | 1995-03-27T05:00:00Z | 1995 | 3 | 2019-07-23T13:26:06Z | 0 | 0 | 090000648055a22b | |||
| FDA-1995-G-0034-0001 | FDA | Hydrophobic Silica for Animal Feeds-CLOSED FDA-1995-G-0034 | FDA/CVM to Degussa Corporation (Keller & Heckman) - Letter | Other | Letter(s) | 1995-03-23T05:00:00Z | 1995 | 3 | 2013-07-27T21:36:27Z | 0 | 0 | 090000648055ae18 | |||
| FDA-1995-P-0045-0002 | FDA | Permit the removal of fat from standardized foods FDA-1995-P-0045 | Acknowledgment Letter from FDA DMB to Lyn O' Brien Nabors | Other | Acknowledgement Letter/Receipt | 1995-03-20T05:00:00Z | 1995 | 3 | 2025-07-21T21:30:16Z | 0 | 0 | 09000064805614fe | |||
| FDA-2020-D-1968-0001 | FDA | FDA-2020-D-1968 | CPG Sec. 355.300 Ion Generating Devices | Other | Guidance | 1995-03-01T05:00:00Z | 1995 | 3 | 2020-09-21T04:00:00Z | 2024-11-06T23:38:56Z | 1 | 0 | 0900006484868f5e | ||
| FDA-1995-P-0415-0001 | FDA | "MDI Albuterol" be submitted to a Joint A.C. for Hearing-CLOSED FDA-1995-P-0415 | Acknowledgment Letter from FDA DDM to Schering Corporation | Other | Acknowledgement Letter/Receipt | 1995-03-01T05:00:00Z | 1995 | 3 | 2017-02-04T19:56:21Z | 0 | 0 | 09000064805a6462 | |||
| FDA-2020-D-1969-0001 | FDA | FDA-2020-D-1969 | CPG Sec. 390.425 Records and Reports; Applicability - 21 CFR 1002.1 | Other | Guidance | 1995-03-01T05:00:00Z | 1995 | 3 | 2020-09-21T04:00:00Z | 2024-11-12T23:25:11Z | 1 | 0 | 0900006484868f60 | ||
| FDA-2010-N-0551-0002 | FDA | FDA-2010-N-0551 | CPG Sec. 393.200 Laser(s) as Medical Devices for Facelift, Wrinkle Removal, Acupuncture, Auricular Stimulation, etc. (CPG 7133.21) | Other | Guidance | 1995-03-01T05:00:00Z | 1995 | 3 | 2020-09-30T04:00:00Z | 2024-11-12T23:26:10Z | 1 | 0 | 09000064848a4277 | ||
| FDA-2020-D-1962-0001 | FDA | FDA-2020-D-1962 | CPG Sec. 300.400 Contamination of Devices Labeled as Sterile | Other | Guidance | 1995-03-01T05:00:00Z | 1995 | 3 | 2020-09-21T04:00:00Z | 2024-11-06T23:38:58Z | 1 | 0 | 0900006484866867 | ||
| FDA-1984-D-0144-0002 | FDA | CYTOTOXIC TESTING FOR ALLERGIC DISEASES CPG FDA-1984-D-0144 | CPG Sec. 370.100 Cytotoxic Testing for Allergic Diseases (CPG 7124.27) | Other | Guidance | 1995-03-01T05:00:00Z | 1995 | 3 | 2020-09-30T04:00:00Z | 2024-11-06T23:39:54Z | 1 | 0 | 09000064848a4275 | ||
| FDA-2020-D-1964-0001 | FDA | FDA-2020-D-1964 | CPG Sec. 335.500 Razor Blades, Manicuring Instruments - Not Considered Devices Under 201(h) | Other | Guidance | 1995-03-01T05:00:00Z | 1995 | 3 | 2020-09-21T04:00:00Z | 2024-11-06T23:38:58Z | 1 | 0 | 090000648486686b | ||
| FDA-2020-D-1970-0001 | FDA | FDA-2020-D-1970 | CPG Sec. 391.200 Warning Statement in Advertisements for High-Intensity Mercury Vapor Discharge Lamps that are not Self-Extinguishing (21 CFR 1040.30(e)(3)*) | Other | Guidance | 1995-03-01T05:00:00Z | 1995 | 3 | 2020-09-21T04:00:00Z | 2024-11-06T23:38:56Z | 1 | 0 | 0900006484868f82 | ||
| FDA-1984-D-0144-0001 | FDA | CYTOTOXIC TESTING FOR ALLERGIC DISEASES CPG FDA-1984-D-0144 | CPG Sec. 370.100 Cytotoxic Testing for Allergic Diseases | Other | Guidance | 1995-03-01T05:00:00Z | 1995 | 3 | 2020-09-30T04:00:00Z | 2024-11-12T23:26:11Z | 1 | 0 | 09000064848a4273 | ||
| FDA-2020-D-1966-0001 | FDA | FDA-2020-D-1966 | CPG Sec. 345.300 Menstrual Sponges | Other | Guidance | 1995-03-01T05:00:00Z | 1995 | 3 | 2020-09-21T04:00:00Z | 2024-11-06T23:38:56Z | 1 | 0 | 0900006484868f5a | ||
| FDA-2020-D-1967-0001 | FDA | FDA-2020-D-1967 | CPG Sec. 355.200 Electrical Muscle Stimulators | Other | Guidance | 1995-03-01T05:00:00Z | 1995 | 3 | 2020-09-21T04:00:00Z | 2024-11-12T23:25:06Z | 1 | 0 | 0900006484868f5c | ||
| FDA-2020-D-1975-0001 | FDA | FDA-2020-D-1975 | CPG Sec. 398.200 Hazardous Diagnostic X-ray Systems | Other | Guidance | 1995-02-28T05:00:00Z | 1995 | 2 | 2020-09-22T04:00:00Z | 2024-11-12T23:25:06Z | 1 | 0 | 0900006484868fa1 | ||
| FDA-1995-P-0024-0001 | FDA | Refuse to Approve Any NDA for RU 486 used as abortifacient FDA-1995-P-0024 | HFA-305 to McKenna & Cuneo | Other | ACK-Acknowledgement Letter | 1995-02-28T05:00:00Z | 1995 | 2 | 2008-05-16T23:07:15Z | 0 | 0 | 0900006480559760 | |||
| FDA-2020-D-1971-0001 | FDA | FDA-2020-D-1971 | CPG Sec. 300.300 Ineffective Devices - 502(f)(I) Labeling Requirements | Other | Guidance | 1995-02-28T05:00:00Z | 1995 | 2 | 2020-09-21T04:00:00Z | 2024-11-12T23:25:11Z | 1 | 0 | 0900006484868f84 | ||
| FDA-2020-D-1972-0001 | FDA | FDA-2020-D-1972 | CPG Sec. 310.100 Pacemaker Reuse | Other | Guidance | 1995-02-28T05:00:00Z | 1995 | 2 | 2020-09-21T04:00:00Z | 2024-11-06T23:38:56Z | 1 | 0 | 0900006484868f86 | ||
| FDA-2020-D-1974-0001 | FDA | FDA-2020-D-1974 | CPG Sec. 397.100 Accuracy Requirements for Indication of Temporal-Maximum Ultrasonic Power, 21 CFR 1050.10(c)(1)(ii) | Other | Guidance | 1995-02-28T05:00:00Z | 1995 | 2 | 2020-09-22T04:00:00Z | 2024-11-06T23:38:57Z | 1 | 0 | 0900006484868f8a | ||
| FDA-1981-N-0012-0014 | FDA | OTC Weight Control Drug Products for Human Use FDA-1981-N-0012 | HFA-305 to Caprice-Grestoke, Ltd. | Other | ACK-Acknowledgement Letter | 1995-02-09T05:00:00Z | 1995 | 2 | 2008-05-30T22:53:16Z | 0 | 0 | 09000064805ae8d9 | |||
| FDA-1981-N-0012-0012 | FDA | OTC Weight Control Drug Products for Human Use FDA-1981-N-0012 | HFA-305 to Caprice-Grestoke, Ltd | Other | ACK-Acknowledgement Letter | 1995-02-02T05:00:00Z | 1995 | 2 | 2008-05-30T22:53:23Z | 0 | 0 | 09000064805ae8d7 | |||
| FDA-1981-N-0012-0013 | FDA | OTC Weight Control Drug Products for Human Use FDA-1981-N-0012 | HFA-305 to Caprice-Grestoke, Ltd | Other | ACK-Acknowledgement Letter | 1995-02-02T05:00:00Z | 1995 | 2 | 2008-05-30T22:53:16Z | 0 | 0 | 09000064805ae8d8 | |||
| FDA-1995-P-0051-0003 | FDA | Ban the Use of Lindane as a Treatment for Lice and Scabies-CLOSED FDA-1995-P-0051 | Acknowledgment Letter from FDA DMB to Cancer Prevention Coalition | Other | Acknowledgement Letter/Receipt | 1995-01-24T05:00:00Z | 1995 | 1 | 2025-09-15T21:40:34Z | 0 | 0 | 0900006480561e5a | |||
| FDA-1978-N-0018-0137 | FDA | Sunscreen Drug Products -OPEN FDA-1978-N-0018 | Letter from FDA CDER to The Cosmetic, Toiletry & Fragrance Association | Other | Letter(s) | 1995-01-17T05:00:00Z | 1995 | 1 | 2019-07-23T13:04:51Z | 0 | 0 | 090000648055a1e9 | |||
| FDA-1978-N-0018-0136 | FDA | Sunscreen Drug Products -OPEN FDA-1978-N-0018 | Letter from FDA CDER to Nonprescription Drug Manufacturers Association | Other | Letter(s) | 1995-01-17T05:00:00Z | 1995 | 1 | 2019-07-22T18:10:56Z | 0 | 0 | 090000648055a1e7 |
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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);