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A00265 Summary:

BILL NOA00265A
 
SAME ASNo Same As
 
SPONSORSteck (MS)
 
COSPNSRNovakhov, DeStefano, Simon, Davila, Bendett, Chang, Levenberg, Weprin, Paulin, Brown K
 
MLTSPNSRWoerner
 
Amd §19.09, Ment Hyg L; amd §3309, Pub Health L
 
Relates to the availability of opioid reversal agents; requires the department of health to make available any formulation and dosage of opioid reversal agent approved by the federal food and drug administration.
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A00265 Text:



 
                STATE OF NEW YORK
        ________________________________________________________________________
 
                                         265--A
 
                               2025-2026 Regular Sessions
 
                   IN ASSEMBLY
 
                                       (Prefiled)
 
                                     January 8, 2025
                                       ___________
 
        Introduced  by  M.  of  A.  STECK,  NOVAKHOV,  DeSTEFANO, SIMON, DAVILA,
          BENDETT, CHANG, LEVENBERG, WEPRIN, PAULIN, K. BROWN -- Multi-Sponsored
          by -- M. of A.  WOERNER -- read once and referred to the Committee  on
          Alcoholism  and  Drug  Abuse  --  committee  discharged, bill amended,
          ordered reprinted as amended and recommitted to said committee
 
        AN ACT to amend the mental hygiene law and the  public  health  law,  in
          relation to the availability of opioid reversal agents
 
          The  People of the State of New York, represented in Senate and Assem-
        bly, do enact as follows:
 
     1    Section 1. Subdivision (l) of section 19.09 of the mental hygiene law,
     2  as added by chapter 434 of the laws of  2021,  is  amended  to  read  as
     3  follows:
     4    (l)(1)  The  office,  in  consultation  with the department of health,
     5  shall maintain on its website a  publicly  available  directory  of  all
     6  distributors  of  opioid  [antagonists]  reversal  agents to the public,
     7  including but not limited to, pharmacies, prevention programs  and  not-
     8  for-profits. As used in this subdivision, the following terms shall have
     9  the following meanings:
    10    (i)  "Opioid"  means  an  opiate  as  defined  in section thirty-three
    11  hundred two of the public health law.
    12    (ii) "Opioid [antagonist] reversal agents" means a  federal  food  and
    13  drug  administration-approved  drug  that, when administered, negates or
    14  neutralizes in whole or in part the pharmacological effects of an opioid
    15  in the body. The [opioid antagonist shall  be  limited  to  naloxone  or
    16  other medications approved by the department of health for this purpose]
    17  department  of health shall make available any formulation and dosage of
    18  opioid reversal agents that are approved by the federal  food  and  drug
    19  administration.
 
         EXPLANATION--Matter in italics (underscored) is new; matter in brackets
                              [ ] is old law to be omitted.
                                                                   LBD00351-02-5

        A. 265--A                           2
 
     1    (iii)  "Purchaser"  means  any  community  organization, municipality,
     2  pharmacy, medical facility, hospital, or any other entity, that accesses
     3  opioid reversal drugs through the New York state standing order.
     4    (2)  The  directory  required by this subdivision shall include and be
     5  searchable by the following information:
     6    (i) addresses of each distributor  of  opioid  [antagonists]  reversal
     7  agents;
     8    (ii)  contact  information,  such as phone numbers or email addresses,
     9  for each distributor;
    10    (iii) services offered by each distributor at each  location  if  more
    11  than  one,  as  well as information providing which opioid [antagonists]
    12  reversal agents are currently available at each distributor;
    13    (iv) special populations served;
    14    (v) insurance providers accepted;
    15    (vi) hours of operation of each distributor;
    16    (vii) contact information of opioid addiction prevention programs; and
    17    (viii) any other information the commissioner deems necessary.
    18    (3) The office may  utilize  an  existing  directory  to  satisfy  the
    19  requirements of this subdivision.
    20    (4) The office shall allow for choice of any formulation and dosage of
    21  opioid  reversal  agents  that are approved by the federal food and drug
    22  administration  in  the  purchase,  distribution  or  authorization   to
    23  prescribe or dispense such products. The department shall cover the cost
    24  of  any  formulation and/or dosage of any federal food and drug adminis-
    25  tration-approved nasal naloxone product.   Any other product  where  the
    26  cost  exceeds  that  of highest-priced nasal naloxone product, that cost
    27  overrun shall be borne by the purchaser.
    28    § 2. Subparagraph (i) of paragraph (a) of  subdivision  3  of  section
    29  3309  of  the public health law, as amended by chapter 42 of the laws of
    30  2014, is amended to read as follows:
    31    (i) "Opioid [antagonist] reversal agents" means a drug approved by the
    32  Food  and  Drug  Administration  that,  when  administered,  negates  or
    33  neutralizes in whole or in part the pharmacological effects of an opioid
    34  in  the  body.  ["Opioid antagonist reversal agents" shall be limited to
    35  naloxone and other medications  approved  by  the  department  for  such
    36  purpose]  The department shall make available any formulation and dosage
    37  of opioid reversal agents that are approved by the federal Food and Drug
    38  Administration.
    39    § 3. Section 3309 of the public health law is amended by adding a  new
    40  subdivision 10 to read as follows:
    41    10.  Any purchase, distribution or authorization to prescribe pursuant
    42  to this section by the commissioner shall allow for choice of any formu-
    43  lation or dosage that is approved by the federal Food and Drug  Adminis-
    44  tration.  The  department shall cover the cost of any formulation and/or
    45  dosage of any federal Food and Drug Administration-approved nasal nalox-
    46  one product.  Any other product where the cost exceeds that of  highest-
    47  priced  nasal  naloxone product, that cost overrun shall be borne by the
    48  purchaser.  Other products where the cost is  lower  than  that  of  the
    49  highest-priced nasal naloxone product shall be borne by the state.
    50    § 4. This act shall take effect immediately.
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