,,iv #aacth ,,congress #ast ,session ,h4 ,,res4 #afa ,,in ,,the ,,house ,,of ,,representatives ,april #ae1 #bjac ,mr4 ,rogers of ,kentucky 7for himself1 ,mr4 ,keating1 ,mr4 ,wolf1 ,mr4 ,rahall1 ,mr4 ,grimm1 ,mr4 ,lynch1 ,mr4 ,tierney1 and ,mr4 ,aderholt7 submitted the following resolution2 which was referred to the ,committee on ,energy and ,commerce ,,resolution ,expressing the sense of the ,house of ,representatives that the ,food and ,drug ,administration should encourage the use of abuse-deterrent formulations of drugs4 ,whereas when abuse-deterrent formulations of a drug have been developed1 approved1 and recognized as effective by the ,food and ,drug ,administration1 the approval and marketing of generic versions that do not have abuse-deterrent features are likely to prevent achievement of the public health purposes of the efforts to develop such abuse-deterrent formulations2 ,whereas the ,office of ,national ,drug ,control ,policy and the ,food and ,drug ,administration have for many years strongly encouraged manufacturers of opioid drug products to develop abuse-deterrent formulations designed to prevent or discourage the abuse or misuse of those products2 ,whereas in response1 several opioid drug manufacturers have developed abuse-deterrent formulations2 ,whereas helping to reduce the level of abuse of opioid drug products is dependent on the widespread adoption of new technologies and approaches to the safer formulation of these drugs2 ,whereas the ,commissioner of ,food and ,drugs has acknowledged that the ,food and ,drug ,administration has the authority under current law to require generic versions of products that have been formulated or reformulated with abuse-deterrent features to have comparable features2 and ,whereas fourteen ,members of ,congress in a bipartisan coalition have cosponsored the ,stop ,tampering with ,prescription ,pills 7,,stopp7 ,act1 which would similarly promote abuse-deterrent technologies in addictive painkillers3 ,now1 therefore1 be it ,that it is the sense of the ,house of ,representatives that the ,food and ,drug ,administration should exercise its acknowledged authority to-- 7#a7 refuse to approve generic versions of non-abuse-deterrent opioid products that have been replaced in the market with abuse-deterrent formulations2 and 7#b7 require generic versions of abuse-deterrent opioid products to be formulated with comparable abuse-deterrent features4