{"data":{"id":"us-in/ic-27-1-24.5-4","jurisdiction":"us-in","citation":"IC 27-1-24.5-4","heading":"\"Generic drug\"","body":"Sec. 4. As used in this chapter, \"generic drug\" means a drug product that is identified by the drug's chemical name and that is:\n(1) accepted by the federal Food and Drug Administration;\n(2) available from at least three (3) sources; and\n(3) therapeutically equivalent to an originating brand name drug.","path":["TITLE 27. INSURANCE","ARTICLE 1. DEPARTMENT OF INSURANCE","Chapter 24.5. Pharmacy Benefit Managers"],"source_url":"https://iga.in.gov/ic/2026/Title_27.html#27-1-24.5-4","current_through":"2026","vintage":"2026","retrieved_at":"2026-09-25T05:39:04Z","sha256":"42269206778b6cee9bffd1adca8ea6c3504f82515431e698e66d100c408590f9","source_id":"us-in","stale":false,"prev":"us-in/ic-27-1-24.5-3","next":"us-in/ic-27-1-24.5-4.5"},"notice":"GroundRules: Original legal text. Not legal advice."}