,,ii #aafth ,,congress #b;d ,session ,s4 #cfce ,,in ,,the ,,senate ,,of ,,the ,,united ,,states ,may #f1 #bjbj,mr4 ,cotton 7for himself1 ,mrs4 ,blackburn1 ,mr4 ,cruz1 ,mr4 ,daines1 and ,mr4 ,scott of ,florida7 introduced the following bill2 which was read twice and referred to the ,committee on ,finance ,a ,,bill ,to require the ,secretary of ,health and ,human ,services to maintain a list of the country of origin of all drugs marketed in the ,united ,states1 to ban the use of ,federal funds for the purchase of1 or reimbursement for1 drugs manufactured in ,china1 and for other purposes4 #a4 ,short title ,this ,act may be cited as the ,protecting ,our ,pharmaceutical ,supply ,chain from ,china ,act of #bjbj4 #b4 ,country of origin of drugs 7a7 ,in general ,subchapter ,a of chapter ,v of the ,federal ,food1 ,drug1 and ,cosmetic ,act 7#ba ,u4,s4,c4 #cea et seq47 is amended by adding at the end the following3 #ebd;,b4 ,registry of drugs produced outside the ,united ,states 7a7 ,in general ,the ,secretary shall compile and maintain a list of all drugs approved under subsection 7c7 or 7j7 of section #eje of this ,act or licensed under subsection 7a7 or 7k7 of section #cea of the ,public ,health ,service ,act1 and any active ingredients in such drugs1 that-- 7#a7 are manufactured outside of the ,united ,states2 and 7#b7 are determined by the ,secretary to be critical to the health and safety of consumers in the ,united ,states4 7b7 ,additional list ,in conjunction with the list described in subsection 7a71 the ,secretary shall compile and maintain a list of drugs included on such list that are exclusively produced in1 or use active or inactive ingredients produced in1 the ,people's ,republic of ,china4 7c7 ,requirement ,the list described in subsection 7a7 shall1 with respect to each drug included on the list1 provide information about the drug's supply chain1 including each step in the supply chain that occurs prior to the drug's importation into the ,united ,states4 4 7b7 ,federal health program purchase of1 or reimbursement for1 drugs 7#a7 ,in general ,notwithstanding any other provision of law1 the ,department of ,health and ,human ,services1 the ,department of ,veterans ,affairs1 the ,department of ,defense1 and any other ,federal health care program 7as defined in section #aabh;,b7f7 of the ,social ,security ,act 7#db ,u4,s4,c4 #acbj;a-#g;b7b771 with respect to the purchase of1 or reimbursement for1 a drug by such agency or program1 the following shall apply3 7,a7 ,by #bjbb1 a purchaser of1 or reimbursor for1 drugs described in this subsection shall purchase drugs or reimburse for drugs only if such drugs contain #fj percent or more of their active pharmaceutical ingredients manufactured in countries-- 7i7 other than the ,people's ,republic of ,china2 and 7ii7 that meet the ,food and ,drug ,administration's health and safety standards4 7,b7 ,by #bjbc1 a purchaser of1 or reimbursor for1 drugs described in this subsection shall purchase drugs or reimburse for drugs only if such drugs contain #ajj percent of their active pharmaceutical ingredients manufactured in countries-- 7i7 other than the ,people's ,republic of ,china2 and 7ii7 that meet the ,food and ,drug ,administration's health and safety standards4 7#b7 ,waivers ,the ,secretary of ,health and ,human ,services may issue waivers of the requirements under paragraph 7#a7 for any agency or program that is unable to meet such requirements and demonstrates a need for the waiver4 ,no waiver may be issued under this paragraph for drugs that are purchased on or after ,january #a1 #bjbe4 7c7 ,labeling requirement ,section #ejb of the ,federal ,food1 ,drug1 and ,cosmetic ,act 7#ba ,u4,s4,c4 #ceb7 is amended by adding at the end the following3 7ee7 ,if it is a drug and its labeling does not specify the country of origin of each active ingredient contained in the drug4 4 #c4 ,temporary #ajj percent expensing for pharmaceutical and medical device manufacturing property 7a7 ,in general ,for purposes of section #afh7k7 of the ,internal ,revenue ,code of #aihf1 in the case of any qualified pharmaceutical and medical device manufacturing property which is placed in service after ,december #ca1 #bjai1 and before ,january #a1 #bjbf-- 7#a7 such property shall be treated as qualified property 7within the meaning of such section71 7#b7 the applicable percentage otherwise determined under section #afh7k77#f7 of such ,code with respect to such property shall be #ajj percent1 and 7#c7 paragraph 7#h7 of such section shall not apply4 7b7 ,qualified pharmaceutical and medical device manufacturing property ,for purposes of this section1 the term qualified pharmaceutical and medical device manufacturing property means any tangible property placed in service in the ,united ,states as part of the construction or expansion of property for the manufacture of drugs 7as defined in section #bja7;g7 of the ,federal ,food1 ,drug1 and ,cosmetic ,act 7#ba ,u4,s4,c4 #cba7;g777 or medical devices 7as defined in section #bja7;h7 of such ,act 7#ba ,u4,s4,c4 #cba7;h7774 7c7 ,termination ,this section shall not apply to any property placed in service after ,december #ca1 #bjbe4 #d4 ,rule of construction ,nothing in this ,act shall be construed to divert the resources of the ,food and ,drug ,administration from responding to the ,,covid-#ai public health emergency4