dockets: FDA-2005-P-0381
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
This data as json
| id | agency_id | title | docket_type | last_modified | object_id | rin | dkabstract | category | subtype | keywords | program | short_title | effective_date | organization | attrs_raw | attr_source |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| FDA-2005-P-0381 | FDA | ANDA Suitability for Diphenoxylate Hydrochloride & Atropine Sulfate Tablets USP 5 mg/0.05.mg-CLOSED | Nonrulemaking | 2021-09-01T01:01:26Z | 0b0000648044be22 | Docket Status: CLOSED 12/15/2008 as per 12/10/2008 Petition Denial. | ["USP", "CDER", "Tablets", "5 mg/0.05.mg", "Atropine Sulfate", "ANDA Suitability", "Diphenoxylate Hydrochloride", "CLOSED"] | CDER | ANDA Suitability for Diphenoxylate Hydrochloride & Atropine Sulfate Tablets | {"displayProperties": [{"name": "abstract", "label": "General Information", "tooltip": "Describes an agency's specific regulatory action; equivalents: Abstract, Description, Docket Subject, Related To, Summary."}, {"name": "legacyId", "label": "Legacy ID", "tooltip": "A pre-FDMS agency specific identifier migrated from a legacy system."}, {"name": "generic", "label": "Docket Item Code", "tooltip": "An agency specific code that identifies the type of document that established the docket (regulatory action)."}, {"name": "program", "label": "Center", "tooltip": "The agency specific program associated with the docket (regulatory action); equivalents: Docket Item Code, Location."}, {"name": "field2", "label": "Docket Status", "tooltip": "Used to Identity that a Docket's Status is Open or Closed"}, {"name": "shortTitle", "label": "Short Title", "tooltip": "A combination of letters and or numbers assigned to an agency's regulatory action for purposes of brevity."}], "keywords": ["USP", "CDER", "Tablets", "5 mg/0.05.mg", "Atropine Sulfate", "ANDA Suitability", "Diphenoxylate Hydrochloride", "CLOSED"], "modifyDate": "2021-09-01T01:01:26Z", "dkAbstract": "Docket Status: CLOSED 12/15/2008 as per 12/10/2008 Petition Denial.", "agencyId": "FDA", "program": "CDER", "shortTitle": "ANDA Suitability for Diphenoxylate Hydrochloride & Atropine Sulfate Tablets", "subType2": null, "title": "ANDA Suitability for Diphenoxylate Hydrochloride & Atropine Sulfate Tablets USP 5 mg/0.05.mg-CLOSED", "generic": "P", "field1": null, "docketType": "Nonrulemaking", "petitionNbr": null, "rin": null, "organization": null, "legacyId": "2005P-0161", "subType": null, "category": null, "field2": "CLOSED", "effectiveDate": null, "objectId": "0b0000648044be22"} | single_get |
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