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HI SB868
Bill
Status
1/25/2017
Primary Sponsor
Ronald Kouchi
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AI Summary
S.B. 868 - Controlled Substances Act Amendments
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Excludes apomorphine, thebaine-derived butorphanol, dextrorphan, nalbuphine, nalmefene, naloxegol, naloxone, and naltrexone and their salts from Schedule I narcotic drug classification under opium and opiate provisions.
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Permits individual practitioners to administer, dispense, and prescribe schedule II, III, IV, or V narcotic drugs approved by the FDA specifically for medically-managed withdrawal treatment or maintenance treatment, provided they comply with federal regulations under 21 CFR § 1301.28 and state registration requirements.
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Allows physicians not registered as narcotic treatment program providers to administer narcotic drugs for acute withdrawal symptom relief during a referral process, limited to one day of medication at a time and not to exceed three days total.
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Clarifies that existing provisions do not restrict physicians or hospital staff from administering narcotic drugs as an incidental adjunct to medical or surgical treatment of non-addiction conditions, or for intractable pain management.
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Takes effect July 1, 2050.
Legislative Description
Relating To The Controlled Substances Act.
Controlled Substances Act
Last Action
Report adopted; Passed Second Reading, as amended (SD 1) and referred to PSM.
2/16/2017