Amends GS 90-85.28(a) concerning the prescription of equivalent drug products, requiring that an equivalent drug must have the US Food and Drug Administration's therapeutic equivalence code on the label of the stock package in order to be dispensed. Makes technical and organizational changes.
Effective October 1, 2015.
|View NCGA Bill Details||2015-2016 Session|
AN ACT ENHANCING STANDARDS FOR PRESCRIBING EQUIVALENT DRUG PRODUCTS BY REQUIRING THESE PRODUCTS TO BE LABELED WITH THE UNITED STATES FOOD AND DRUG ADMINISTRATION THERAPEUTIC EQUIVALENCE CODE.Intro. by Bingham.
Status: Ref To Com On Rules and Operations of the Senate (Senate Action) (Mar 11 2015)
Bill S 234 (2015-2016)Summary date: Mar 10 2015 - More information