{"database": "openregs", "table": "federal_register", "rows": [["E8-18127", "Draft Guidance for Industry on Residual Solvents in Drug Products Marketed in the United States; Availability", "Notice", "The Food and Drug Administration (FDA) is announcing the availability of a draft guidance for industry entitled \"Control of Residual Solvents in Drug Products Marketed in the United States.\" On July 1, 2008, the United States Pharmacopeia (USP) published a new test requirement for the control of residual solvents, General Chapter <467> \"Residual Solvents,\" which replaced USP General Chapter <467> \"Organic Volatile Impurities.\" The change affects all compendial drug products marketed in the United States. This draft guidance reflects FDA's recommendations on how to comply with those USP changes.", "2008-08-07", 2008, 8, "https://www.federalregister.gov/documents/2008/08/07/E8-18127/draft-guidance-for-industry-on-residual-solvents-in-drug-products-marketed-in-the-united-states", "https://www.govinfo.gov/content/pkg/FR-2008-08-07/pdf/E8-18127.pdf", "Health and Human Services Department; Food and Drug Administration", "221,199", "The Food and Drug Administration (FDA) is announcing the availability of a draft guidance for industry entitled \"Control of Residual Solvents in Drug Products Marketed in the United States.\" On July 1, 2008, the United States Pharmacopeia (USP)...", null]], "columns": ["document_number", "title", "type", "abstract", "publication_date", "pub_year", "pub_month", "html_url", "pdf_url", "agency_names", "agency_ids", "excerpts", "regulation_id_numbers"], "primary_keys": ["document_number"], "primary_key_values": ["E8-18127"], "units": {}, "query_ms": 3.514306154102087, "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"}