New Mexico 2025 Regular Session

New Mexico House Bill HB505 Compare Versions

Only one version of the bill is available at this time.
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2828 HOUSE BILL 505
2929 57
3030 TH LEGISLATURE
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4242 FIRST SESSION
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4545 2025
4646 INTRODUCED BY
4747 Cristina Parajón and Antoinette Sedillo Lopez
4848 AN ACT
4949 RELATING TO OPIOIDS; REQUIRING RETAIL PHARMACIES TO KEEP STOCKS
5050 OF CERTAIN TYPES OF DRUGS THAT TREAT OPIOID USE DISORDER;
5151 REQUIRING WHOLESALE DRUG DISTRIBUTORS TO REPORT INSTANCES IN
5252 WHICH THE DISTRIBUTORS DO NOT FILL ORDERS FOR BUPRENORPHINE
5353 MADE BY RETAIL PHARMACIES; REQUIRING REPORTS; PROVIDING
5454 PENALTIES.
5555 BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF NEW MEXICO:
5656 SECTION 1. A new section of the New Mexico Drug, Device
5757 and Cosmetic Act is enacted to read:
5858 "[NEW MATERIAL] BUPRENORPHINE STOCKING REQUIREMENTS.--
5959 A. At least once every thirty days, each retail
6060 pharmacy that stocks controlled substances shall compute the
6161 retail pharmacy's minimum daily buprenorphine stocking
6262 requirement by determining the average amount of buprenorphine
6363 .229397.6 underscored material = new
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9090 dispensed per day in the previous thirty days, rounding to the
9191 nearest milligram. Each retail pharmacy shall maintain a stock
9292 of buprenorphine sufficient to satisfy the minimum daily
9393 buprenorphine stocking requirement, plus at least three
9494 additional prescriptions for buprenorphine, including at least
9595 one prescription for buprenorphine that is a buprenorphine
9696 monoproduct and one prescription for buprenorphine that is a
9797 buprenorphine-naloxone combination product. A retail pharmacy
9898 that fails to satisfy the stocking requirements of this section
9999 is not in violation of this section if the retail pharmacy
100100 takes any of the following actions within three days of failing
101101 to satisfy the stocking requirements:
102102 (1) ordering a replacement stock of
103103 buprenorphine sufficient to satisfy the stocking requirements
104104 of this section; or
105105 (2) requesting a wholesale drug distributor to
106106 increase the retail pharmacy's allotment of buprenorphine, and:
107107 (a) once the wholesale drug distributor
108108 approves the request, ordering a replacement stock of
109109 buprenorphine within three days of receiving the approval; or
110110 (b) the wholesale drug distributor
111111 denies the request.
112112 B. A retail pharmacy shall maintain records of the
113113 retail pharmacy's minimum daily buprenorphine stocking
114114 requirements. Records shall be maintained for a period of at
115115 .229397.6
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143143 least three years from the date of the record and may be
144144 inspected as required by authorized agents of the board.
145145 C. A wholesale drug distributor shall report to the
146146 board on a monthly basis, in a form and manner prescribed by
147147 the board, each instance in which the wholesale drug
148148 distributor:
149149 (1) denied, in whole or in part, an order for
150150 buprenorphine submitted by a retail pharmacy;
151151 (2) delayed an order for buprenorphine
152152 submitted by a retail pharmacy due to the retail pharmacy's
153153 threshold of buprenorphine; or
154154 (3) denied a request by a retail pharmacy to
155155 increase the retail pharmacy's threshold of buprenorphine.
156156 D. A report submitted by a wholesale drug
157157 distributor pursuant to this subsection shall include:
158158 (1) the name of the retail pharmacy affected;
159159 (2) the date on which the retail pharmacy
160160 submitted the order for buprenorphine or requested an increase
161161 to the retail pharmacy's threshold of buprenorphine;
162162 (3) the date on which the wholesale drug
163163 distributor denied or delayed the retail pharmacy's order for
164164 buprenorphine or denied the requested increase in the retail
165165 pharmacy's threshold of buprenorphine;
166166 (4) the reason the wholesale drug distributor
167167 denied or delayed the retail pharmacy's order for buprenorphine
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196196 or denied the requested increase in the retail pharmacy's
197197 threshold of buprenorphine; and
198198 (5) any other information required by the
199199 board.
200200 E. The board shall submit data gathered pursuant to
201201 this section to the department of health. The department of
202202 health shall analyze the data and publish a biannual report on
203203 access to buprenorphine in retail pharmacies. The report shall
204204 include:
205205 (1) information on the frequency with which
206206 each wholesale drug distributor:
207207 (a) denied a retail pharmacy's order for
208208 buprenorphine;
209209 (b) delayed a retail pharmacy's order
210210 for buprenorphine due to the retail pharmacy's threshold of
211211 buprenorphine; or
212212 (c) denied a retail pharmacy's requested
213213 increase in the retail pharmacy's threshold of buprenorphine;
214214 (2) aggregated data on the reasons reported by
215215 wholesale drug distributors for denying a retail pharmacy's
216216 order for buprenorphine or a request by a retail pharmacy to
217217 increase the retail pharmacy's threshold of buprenorphine;
218218 (3) a description of how denials or delays of
219219 retail pharmacy orders for buprenorphine affected access to
220220 buprenorphine;
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249249 (4) a description of how denials of retail
250250 pharmacy requests to increase their threshold of buprenorphine
251251 affected access to buprenorphine;
252252 (5) geographic and demographic disparities in
253253 access to buprenorphine in retail pharmacies, to the extent the
254254 data is available;
255255 (6) the impact of insufficient access to
256256 buprenorphine in retail pharmacies on initiation of and
257257 retention in treatment for opioid use disorder, overdose
258258 morbidity and mortality and other health outcomes associated
259259 with substance use disorder; and
260260 (7) any other relevant information.
261261 F. Reports published pursuant to Subsection E of
262262 this section shall comply with state and federal privacy and
263263 confidentiality laws, rules and regulations.
264264 G. The board may impose the following penalties on
265265 retail pharmacies that violate this section:
266266 (1) for a first or second violation, notice of
267267 the violation that includes information on the requirements to
268268 comply with this section; and
269269 (2) for a third violation or any subsequent
270270 violation within a thirty-six-month period following the
271271 previous violation, a fine not to exceed two thousand five
272272 hundred dollars ($2,500).
273273 H. The board may impose the following penalties on
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302302 wholesale drug distributors that violate this section:
303303 (1) for a first violation, notice of the
304304 violation that includes information on the requirements to
305305 comply with this section; and
306306 (2) for a second violation or any subsequent
307307 violation within a thirty-six-month period following the
308308 previous violation, a fine not to exceed ten thousand dollars
309309 ($10,000).
310310 I. As used in this section:
311311 (1) "buprenorphine" means the drug
312312 buprenorphine, including any official, generic or chemical name
313313 used to describe buprenorphine prescribed for the treatment of
314314 opioid use disorder;
315315 (2) "minimum daily buprenorphine stocking
316316 requirement" means the average number of milligrams of
317317 buprenorphine dispensed by a retail pharmacy per day over a
318318 thirty-day period, in formulations, dosages and brand names
319319 consistent with the prescriptions for buprenorphine dispensed
320320 by the retail pharmacy during the thirty-day period;
321321 (3) "prescription for buprenorphine" means
322322 sufficient buprenorphine in tablet or film form to provide a
323323 patient with twenty-four milligrams per day for two weeks;
324324 (4) "retail pharmacy" means a pharmacy
325325 physically located, and licensed to dispense drugs, in the
326326 state; and
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355355 (5) "wholesale drug distributor" means a
356356 person licensed to engage in the wholesale distribution of
357357 prescription drugs in the state."
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