{"database": "openregs", "table": "documents", "rows": [["EPA-HQ-OW-2003-0007-0003", "EPA", "EPA-HQ-OW-2003-0007", "Pharmaceutical Manufacturing Point Source Category Interim Final Rulemaking.  Vol. 41, No. 223.", "Rule", "Federal Register Document", "2003-02-26T05:00:00Z", 2003, 2, null, null, "2008-01-08T21:08:51Z", "50676", 0, 0, "09000064800c2a58"]], "columns": ["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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["EPA-HQ-OW-2003-0007-0003"], "units": {}, "query_ms": 0.4035679157823324, "source": "Federal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"}