{"database": "openregs", "table": "dockets", "rows": [["DEA-2008-0001", "DEA", "Registration Requirements for\r\nImporters and Manufacturers of\r\nPrescription Drug Products Containing\r\nEphedrine, Pseudoephedrine, or\r\nPhenylpropanolamine", "Rulemaking", "2021-12-02T01:00:36Z", "0b000064803e8488"]], "columns": ["id", "agency_id", "title", "docket_type", "last_modified", "object_id"], "primary_keys": ["id"], "primary_key_values": ["DEA-2008-0001"], "units": {}, "query_ms": 1.7331349663436413, "source": "Federal Register API & Regulations.gov API", "source_url": "https://www.federalregister.gov/developers/api/v1", "license": "Public Domain (U.S. Government data)", "license_url": "https://www.regulations.gov/faq"}