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Assembly Bill A6054

2009-2010 Legislative Session

Relates to certain labelling requirements when substitute drug products are dispensed

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Archive: Last Bill Status - In Assembly Committee

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2009-A6054 (ACTIVE) - Details

Current Committee:
Assembly Consumer Affairs And Protection
Law Section:
Education Law
Laws Affected:
Amd ยง6816-a, Ed L
Versions Introduced in Other Legislative Sessions:
2011-2012: A3840
2013-2014: A5447
2015-2016: A4785
2017-2018: A2761
2019-2020: A4571
2021-2022: A2258
2023-2024: A4804

2009-A6054 (ACTIVE) - Summary

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

2009-A6054 (ACTIVE) - Bill Text download pdf 

                            
                    S T A T E   O F   N E W   Y O R K
________________________________________________________________________

                                  6054

                       2009-2010 Regular Sessions

                          I N  A S S E M B L Y

                            February 24, 2009
                               ___________

Introduced by M. of A. BUTLER, ALFANO, KOLB, FINCH -- Multi-Sponsored by
  --  M.  of  A.  CALHOUN,  OAKS,  TOWNSEND, WEISENBERG -- 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.
  S  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.
                                                           LBD05450-01-9

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