All Roll Calls
Yes: 189 • No: 0
Sponsored By: Michael Crider (Republican)
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5 provisions identified: 0 benefits, 1 costs, 4 mixed.
Beginning July 1, 2026, a practitioner must check INSPECT or the patient’s integrated health record before prescribing an opioid or benzodiazepine. Exceptions apply for no Internet at the practice (with a waiver), when a patient is completing another practitioner’s prescription while inpatient or in observation, during a database outage (document the attempt), and for hospice patients. For patients under a pain management contract, checking is required no more than once every 90 days. A practitioner who checks in good faith is immune from civil liability, except for gross negligence or intentional misconduct.
Beginning July 1, 2026, retail pharmacies may not dispense ephedrine, pseudoephedrine, or a controlled drug to someone the dispenser does not personally know. This rule applies only in retail pharmacy settings. It can limit pickup for people without an existing relationship with that pharmacy.
Beginning July 1, 2026, dispensers must send INSPECT data within 24 hours after dispensing, or by the next business day if closed. Reports must include key fields like patient name, ID number, birth date, NDC, date, quantity, days’ supply, prescriber and dispenser DEA numbers, and whether the prescription was oral or written. Upload through the INSPECT website or another board‑approved electronic method. The law defines what counts as a “dispense” and sets clear carve‑outs: no reporting when a drug is given directly to a patient and no reporting for a practitioner’s 72‑hour or less supply of a Schedule II–V drug. A separate exemption also applies to veterinary dispensings of 72 hours or less.
Beginning July 1, 2026, INSPECT data also covers clinical alerts, overdose or poisoning reports, and whether someone is in an opioid treatment program. The board may share data with the state health department and the family and social services office to help active controlled‑substance investigations and to prevent overdoses. Opioid treatment programs must get patient consent under federal rules (42 CFR 2.36 and 2.31) before reporting to INSPECT.
Beginning July 1, 2026, the pharmacy board may require a single, non‑duplicable prescription form for ephedrine, pseudoephedrine, and other controlled drugs. The rule does not apply to prescriptions filled at hospital pharmacies with a Category II permit or to prescriptions for enrolled patients in certain state‑licensed facilities. The board cannot require multi‑copy forms or different forms for different drugs.
Michael Crider
Republican • Senate
Brad Barrett
Republican • House
Cindy Ledbetter
Republican • House
Ed Charbonneau
Republican • Senate
Lori Goss-Reaves
Republican • House
All Roll Calls
Yes: 189 • No: 0
Senate vote • 2/25/2026
Roll Call 287 on SB0262.04.COMH.CON01
Yes: 47 • No: 0 • Other: 2
House vote • 2/23/2026
Roll Call 312 on SB0262.04.COMH
Yes: 94 • No: 0 • Other: 1
Senate vote • 1/28/2026
Roll Call 127 on SB0262.03.ENGS
Yes: 48 • No: 0
Public Law 133
Signed by the Governor
Signed by the President Pro Tempore
Signed by the President of the Senate
Signed by the Speaker
Senate concurred with House amendments; Roll Call 287: yeas 47, nays 0
Motion to concur filed
Returned to the Senate with amendments
Third reading: passed; Roll Call 312: yeas 94, nays 0
Second reading: ordered engrossed
Committee report: amend do pass, adopted
First reading: referred to Committee on Public Health
Referred to the House
Third reading: passed; Roll Call 127: yeas 48, nays 0
Cosponsors: Representatives Barrett, Ledbetter
House sponsor: Representative Goss-Reaves
Amendment #2 (Crider) prevailed; voice vote
Second reading: amended, ordered engrossed
Senator Charbonneau added as second author
Committee report: amend do pass, adopted
Authored by Senator Crider
First reading: referred to Committee on Health and Provider Services
Engrossed Senate Bill (H)
Enrolled Senate Bill (S)
Introduced Senate Bill (S)
Senate Bill (S)