Assembly Bill A2761

2017-2018 Legislative Session

Relates to certain labelling requirements when substitute drug products are dispensed

download bill text pdf

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Archive: Last Bill Status - In Assembly Committee

  • Introduced
    • In Committee Assembly
    • In Committee Senate
    • On Floor Calendar Assembly
    • On Floor Calendar Senate
    • Passed Assembly
    • Passed Senate
  • Delivered to Governor
  • Signed By Governor

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2017-A2761 (ACTIVE) - Details

Current Committee:
Assembly Consumer Affairs And Protection
Law Section:
Education Law
Laws Affected:
Amd §6816-a, Ed L
Versions Introduced in Other Legislative Sessions:
2009-2010: A6054
2011-2012: A3840
2013-2014: A5447
2015-2016: A4785
2019-2020: A4571
2021-2022: A2258
2023-2024: A4804

2017-A2761 (ACTIVE) - Summary

Requires the brand name of a prescribed drug to be indicated on the label when substitute drug products are dispensed.

2017-A2761 (ACTIVE) - Bill Text download pdf 

                            
 
                     S T A T E   O F   N E W   Y O R K
 ________________________________________________________________________
 
                                   2761
 
                        2017-2018 Regular Sessions
 
                           I N  A S S E M B L Y
 
                             January 23, 2017
                                ___________
 
 Introduced by M. of A. BUTLER -- read once and referred to the Committee
   on Consumer Affairs and Protection
 
 AN  ACT  to amend the education law, in relation to certain requirements
   when substitute drug products are dispensed
 
   THE PEOPLE OF THE STATE OF NEW YORK, REPRESENTED IN SENATE AND  ASSEM-
 BLY, DO ENACT AS FOLLOWS:

   Section  1.  Paragraph  (c)  of subdivision 1 of section 6816-a of the
 education law, as added by chapter 776 of the laws of 1977,  is  amended
 to read as follows:
   (c)  The pharmacist shall indicate on the label affixed to the immedi-
 ate container in which the drug  is  sold  or  dispensed  the  name  and
 strength  of the drug product and its manufacturer unless the prescriber
 specifically states otherwise, AND SHALL ALSO INDICATE THE BRAND NAME OF
 THE DRUG PRESCRIBED. The pharmacist shall  record  on  the  prescription
 form  the brand name or the name of the manufacturer of the drug product
 dispensed.
   § 2. This act shall take effect on the thirtieth day  after  it  shall
 have become a law.
 
 
 
 
 
  EXPLANATION--Matter in ITALICS (underscored) is new; matter in brackets
                       [ ] is old law to be omitted.
                                                            LBD01358-01-7

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