{"database": "openregs", "table": "federal_register", "rows": [["00-15556", "Determination That Fluoxetine Hydrochloride 20-Milligram Tablets Were Not Withdrawn From Sale for Reasons of Safety or Effectiveness", "Notice", "The Food and Drug Administration (FDA) is announcing its determination that fluoxetine hydrochloride 20-milligram (mg) tablets (Prozac<Register>) were not withdrawn from sale for reasons of safety or effectiveness. This determination will allow FDA to approve abbreviated new drug applications (ANDA's) for fluoxetine hydrochloride 20-mg tablets.", "2000-06-21", 2000, 6, "https://www.federalregister.gov/documents/2000/06/21/00-15556/determination-that-fluoxetine-hydrochloride-20-milligram-tablets-were-not-withdrawn-from-sale-for", "https://www.govinfo.gov/content/pkg/FR-2000-06-21/pdf/00-15556.pdf", "Health and Human Services Department; Food and Drug Administration", "221,199", "The Food and Drug Administration (FDA) is announcing its determination that fluoxetine hydrochloride 20-milligram (mg) tablets (Prozac<Register>) were not withdrawn from sale for reasons of safety or effectiveness. This determination will allow FDA to...", 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": ["00-15556"], "units": {}, "query_ms": 0.5021860124543309, "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"}