{"data":{"id":"us-nm/27-2c-2","jurisdiction":"us-nm","citation":"27-2C-2","heading":"Definitions.","body":"As used in the Pharmaceutical Supplemental Rebate Act:\nA. \"authority\" or \"department\" means the health care authority;\nB. \"labeler\" means a person that receives prescription drugs from a manufacturer or wholesaler and repackages those drugs for later retail sale and that has a labeler code from the federal food and drug administration;\nC. \"manufacturer\" means a manufacturer of prescription drugs as defined in 42 U.S.C. 1396r-8(k)(5), including a subsidiary or affiliate of a manufacturer;\nD. \"medicaid\" means the joint federal-state health coverage program pursuant to Title 19 or Title 21 of the federal Social Security Act;\nE. \"participating retail pharmacy\" means a retail pharmacy or other business licensed to dispense prescription drugs that participates in the state medicaid program;\nF. \"secretary\" means the secretary of health care authority; and\nG. \"wholesaler\" means a business licensed to distribute prescription drugs in the state.","path":["Chapter 27 - Public Assistance","ARTICLE 2C Pharmaceutical Supplemental Rebate"],"source_url":"https://nmonesource.com/nmos/nmsa-unanno/en/item/18527/index.do","current_through":"2026-07-01","vintage":"","retrieved_at":"2026-09-03T15:02:19Z","sha256":"72e1b907b5f166a849312471e1acaafda3158e829b6bcc325a5a6154a0effd54","source_id":"us-nm","stale":false,"prev":"us-nm/27-2c-1","next":"us-nm/27-2c-3"},"notice":"GroundRules: Original legal text. Not legal advice."}