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F I S C A L I M P A C T R E P O R T





SPONSOR: Heaton DATE TYPED: 02/22/01 HB 502
SHORT TITLE: Amend NM Drug, Device & Cosmetic Act SB
ANALYST: Rael


APPROPRIATION



Appropriation Contained
Estimated Additional Impact
Recurring

or Non-Rec

Fund

Affected

FY01 FY02 FY01 FY02

No Fiscal Impact



(Parenthesis ( ) Indicate Expenditure Decreases)



Relates to SB 678



SOURCES OF INFORMATION



Attorney General's Office (AGO)

Department of Health (DOH)



SUMMARY



Synopsis of Bill



The Amend NM Drug, Device and Cosmetic Act would enact a new section of the New Mexico Drug, Device and Cosmetic Act to prohibit discrimination against reimported drugs that are in compliance with federal law, specifically allowing the importation of certain drugs.



Significant Issues



Currently, drugs may be manufactured in the United States and then shipped to a foreign country for sale. When U.S. distributors attempt to purchase them from the foreign country for use in the U.S. (reimportation), the standards are often stricter for these drugs, causing the price of the drug to be higher for the U.S. consumer. This Bill prohibits the New Mexico Board of Pharmacy from requiring stricter standards for a reimported drug, thus reducing the cost of the medication to the N.M. consumer.



OTHER SUBSTANTIVE ISSUES



The intent of HB 502 would be to lower overall prescription costs to the consumer. The Department of Health reports that HB 502 has the potential to lower health insurance rates in New Mexico.



The Attorney General reports that there is similar federal legislation that has not been utilized, because it requires the Drug Enforcement Agency to first adopt regulations. The DEA has not yet done so.

FAR/ar