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Minnesota Board
of Pharmacy
FREQUENTLY ASKED QUESTIONS
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I have received
e-mail (spam) and/or a fax from a company claiming to be a pharmacy
licensed by the Minnesota Board of Pharmacy. (Or, I have visited a website
that displays a license supposedly issued by the Board).
Has the Board issued a license to this
company or website? If not, what can the Board do to stop the company from
sending me spam or faxes? Can the Board make them remove charges from my
credit card? I have received a telephone call from someone claiming to work
for a licensed pharmacy who encourages me to order from them or asks me for
credit card information. Can the Board stop them from calling me?
Minnesota Statutes § 151.461 prohibits gifts to
practitioners by drug wholesalers and manufacturers. Can you provide
additional information about this law?
Minnesota Rule 6800.0700 requires a community/retail pharmacy to have an
area where consultation between the patient and the pharmacist may be
conducted with an assurance of privacy. Does the Board have
recommendations as to how a pharmacy can comply with this rule?
Where can I find information about the new methamphetamine/pseudoephedrine
law?
What information can be changed (or
added) to a schedule II prescription and schedule III- V
prescriptions by a pharmacist?
06/08/2011
Is there a time limit between the date a prescription for a schedule II drug
is issued and the date when it may be filled?
Is there a six month/five refill limit on schedule V drugs?
Can prescriptions be transferred more than once in Minnesota?
I just received a prescription for methadone. Can I dispense it?
Can I fill or refill a prescription from an out of state prescriber?
Can I fill a prescription for a schedule II drug written by a mid-level
practitioner?
How long must I keep prescription records?
Can I accept a new prescription via a facsimile machine?
Can I mail prescription medications containing narcotics or other
controlled substances?
Where can I find a chart showing the daily
limits for retail pseudoephedrine sales?
I allowed my license to practice pharmacy in Minnesota to lapse and now I
want it reinstated. What do I need to do?
Does
your Board have license verification on the Internet?
Does your Board of Pharmacy license
or register medical device or medical supply manufacturers, wholesale
distributors, suppliers or retailers?
8/3/2011
Where can I find out information about the Board’s continuing education requirement for pharmacy technicians?
2/21/2012
- I have received e-mail (spam) and/or
a fax from a company claiming to be a pharmacy licensed by the Minnesota
Board of Pharmacy. (Or, I have visited a website that displays a license
supposedly issued by the Board). Has the Board issued a license to this
company or website? If not, what can the Board do to stop the company from
sending me spam or faxes? Can the Board make them remove charges from my
credit card? I have received a telephone call from someone claiming to work
for a licensed pharmacy who encourages me to order from them or asks me for
credit card information. Can the Board stop them from calling me?
Answer.
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- MINNESOTA STATUTES § 151.461 PROHIBITS GIFTS
TO PRACTITIONERS BY DRUG WHOLESALERS AND MANUFACTURERS. CAN YOU PROVIDE
ADDITIONAL INFORMATION ABOUT THIS LAW?
Yes, the recommendations can be found
here.
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- MINNESOTA RULE 6800.0700 REQUIRES A
COMMUNITY/RETAIL PHARMACY TO HAVE AN AREA WHERE CONSULTATION BETWEEN THE
PATIENT AND THE PHARMACIST MAY BE CONDUCTED WITH AN ASSURANCE OF
PRIVACY. DOES THE BOARD HAVE RECOMMENDATIONS AS TO HOW A PHARMACY
CAN COMPLY WITH THIS RULE?
Yes, the recommendations can be found
here.
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- WHAT INFORMATION CAN BE CHANGED (OR ADDED) TO A SCHEDULE II
PRESCRIPTION AND SCHEDULE III - V PRESCRIPTIONS BY A PHARMACIST?
06/08/2011
For CII prescriptions the DEA
is currently deferring to the states on this issue. The Minnesota Board
of Pharmacy has adopted this position:
The pharmacist may add or change the patient’s address upon verification.
The pharmacist may add or change the dosage form, drug strength, drug
quantity, directions for use, or issue date only after consultation with and
with the agreement of the prescribing practitioner. Such consultations and
corresponding changes should be noted by the pharmacist on the prescription.
The
pharmacist may add the DEA number of the prescriber upon determining that
the prescription is legally valid. The pharmacist is never permitted to make changes to the patient’s name,
controlled substance prescribed (except for generic substitution permitted
by state law) or the prescriber’s signature.
Note that you must contact the prescriber in order to make changes on a
schedule II prescription.
For CIII - CV prescriptions the pharmacist may add or change the patient’s address upon verification.
The pharmacist may add or change the dosage form, drug strength, drug
quantity, directions for use, or issue date only after consultation with and
with the agreement of the prescribing practitioner. Such consultations and
corresponding changes should be noted by the pharmacist on the prescription.
The
pharmacist may add the DEA number of the prescriber upon determining that
the prescription is legally valid. The pharmacist is never permitted to make changes to the patient’s name,
controlled substance prescribed (except for generic substitution permitted
by state law) or the prescriber’s signature.
- IS THERE A TIME LIMIT BETWEEN THE DATE A PRESCRIPTION FOR A
SCHEDULE II DRUG IS ISSUED AND THE DATE WHEN IT MAY BE FILLED?
There is no time limit under federal law, however under Minnesota Rules,
a one year limit from the date of issue exists for all prescriptions.
DEA's recent rule change allowing for the issuance of multiple
prescriptions authorizing the patient to
receive a total of up to a 90-day supply of a Schedule II controlled
substance have not
added a limit of 90 days from the date of issue that a pharmacy may fill
these prescriptions. It has limited how soon a pharmacy
may fill a prescription for a Schedule II controlled substance to not
earlier than the date specified on the prescription by the prescriber.
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- IS THERE A SIX MONTH/FIVE REFILL LIMIT ON SCHEDULE V DRUGS?
No. While federal rules
provide that prescriptions for drugs in Schedules III and IV cannot be filled or refilled
longer than six months after the date they were issued,
prescriptions for Schedule V drugs can be refilled, as authorized, up to one year
from the date of issue state limit. Keep in mind that federal
Schedule V codeine containing cough syrups are Schedule III in Minnesota
and under Minnesota
Statute 152.11 are subject to the six month/five refill limitation.
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- CAN PRESCRIPTIONS BE TRANSFERRED MORE THAN ONCE IN MINNESOTA?
Prescriptions for non-controlled drugs can be transferred from one pharmacy to another
indefinitely providing that refill authorizations do exist and the transfers are properly
recorded. However, there are restrictions on controlled substances. Minnesota Rule
6800.3120 Subp. 2. states: A pharmacy may transfer prescription information for the
purpose of refilling a prescription if the information is communicated directly by one
licensed pharmacist to another. Schedule II prescriptions may not be transferred.
Schedules III-V prescriptions may only be transferred in accordance with the limitations
placed on such transfers by the Drug Enforcement Administration (DEA). Federal regulation 21 CFR1306.25(a) permits multiple transfers of controlled
substances, providing authorization exists, only for those pharmacies that share a
real time on-line electronic database. Other pharmacies are limited to only one
transfer under federal rules.
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- I JUST RECEIVED A PRESCRIPTION FOR METHADONE. CAN I DISPENSE IT?
Methadone can be dispensed by a pharmacist pursuant to a prescription issued for analgesic
purposes. The following article was taken from the May, 1996 State Board News and
addresses this issue in detail:
Methadone and the Community Pharmacy.
In December 1972, the commissioner of Food and Drugs prohibited the shipment to, or
receipt or dispensing of, methadone by community pharmacies for analgesic purposes (37
Fed. Reg. 26,790). The regulations adopted by the federal Food and Drug Administration
(FDA) established the conditions for use of the drug by methadone treatment programs to
detoxify and maintain narcotic addicts and by hospitals for analgesic purposes on a
temporary basis. Both the drug treatment programs and the hospital pharmacies had to be
approved by FDA to purchase, receive, and use methadone.
On July 9, 1976, these restrictions were lifted by FDA (41 Fed. Reg. 28,261). Accordingly,
all licensed pharmacies can purchase, receive, and dispense methadone for analgesic
purposes after this date. However, questions received by the Board office indicate that
many practicing pharmacists are not aware of the fact that methadone has been available
for dispensing for analgesic purposes by community pharmacists since 1976.
Federal regulations do not permit the prescribing of methadone for purposes of detoxifying
or maintaining a narcotic addict. Prescriptions issued for this purpose are illegal and do
not authorize pharmacists to dispense methadone for these purposes. The federal
regulations require that methadone may only be administered for these purposes by drug
treatment programs approved by the FDA (21CFR 1306.07).
21 CFR 1306.04 (Purpose of issue of prescription) provides that "a prescription may
not be issued for the purpose of dispensing of narcotic drugs in any schedule for
detoxification treatment" or "maintenance treatment". These terms are
defined as follows in Section 102 of the federal Controlled Substance Act (21 U.S.C. 802).
21 USC 802 Definitions.
As used in this subchapter:
(29) The term "maintenance treatment" means the dispensing, for a period in
excess of twenty-one days, of a narcotic drug in the treatment of an individual for
dependence upon heroin or other morphine-like drugs.
(30) The term "detoxification treatment" means the dispensing, for a period not
in excess of one hundred and eighty days, of a narcotic drug in decreasing doses to an
individual in order to alleviate adverse physiological or psychological effects incident
to withdrawal from the continuous or sustained use of a narcotic drug and as a method of
bringing the individual to a narcotic drug-free state within such period.
Pharmacists practicing in community pharmacies have received prescriptions in which it was
obvious that the prescriber was attempting to provide "detoxification treatment"
for a patient who has become dependent on morphine-like drugs. These prescriptions are not
valid and narcotics should not be dispensed under these circumstances. The pharmacist
needs to contact the physician to inquire about their intent and to inform them about
federal regulations governing the use of narcotics to detoxify the patient.
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- CAN I FILL OR REFILL A PRESCRIPTION FROM AN OUT OF STATE
PRESCRIBER?
8/1/2004
Minnesota pharmacies may legally fill or refill, providing refill authorizations
exist, prescriptions from prescribers practicing in any state. If the prescription is
for a controlled substance in Schedule II, III or IV, the practitioner must be
licensed to prescribe controlled substances by the state in which the
prescription is issued and have a current federal Drug Enforcement
Administration registration number. Schedule II prescriptions, or course, cannot be refilled.
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- CAN I FILL A PRESCRIPTION FOR A SCHEDULE II DRUG WRITTEN BY A
MID-LEVEL PRACTITIONER?
Yes, provided that the mid-level practitioner has a valid agreement with a licensed
practitioner that delegates the prescribing of that drug to the mid-level practitioner and
the mid-level practitioner has a current federal drug enforcement registration number.
Note, the federal drug enforcement registration number must be that of the
mid-level practitioner, not that of the delegating licensed practitioner.
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- HOW LONG MUST I KEEP PRESCRIPTION RECORDS?
1/1/2006
Minnesota law requires prescription records to be kept for a minimum of two years. Federal
DEA regulations also require that controlled substance records be kept for a minimum of
two years. The Food and Drug Administration (FDA) maintains that in its enforcement of the
Federal Food, Drug, and Cosmetic Act, it may request records of drug distribution dating
back five years. As of January 1, 2005 the Medicare Modernization
Act of 2003 requires prescription records to be kept for ten years. Pharmacists should also seek the advice of their attorney for an
answer to this question.
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- CAN I ACCEPT A NEW PRESCRIPTION VIA A FACSIMILE MACHINE?
Minnesota Rules do
allow a pharmacy to accept a prescription transmitted by facsimile from the prescriber to
the pharmacy, provided the facsimile document is readily readable for at least five years.
Facsimile orders for controlled substance in Schedules II, III, and IV can only be
accepted if in compliance with federal DEA rules.
Federal regulations do allow for the transmission of a prescription to a pharmacy by a
practitioner, or the practitioneer's agent, for controlled substances in Schedule III, IV
and V. (21CFR1306.21,a) The following federal regulations apply
to prescriptions for Schedule II controlled substances. (21CFR1306.11)
... A prescription for a Schedule II controlled substance may be transmitted by the
practitioner or the practitioner's agent to a pharmacy via facsimile equipment, provided
that the original written, signed prescription is presented to the pharmacist for review
prior to the actual dispensing of the controlled substance, except as noted in paragraph
(e), (f), or (g) of this section.
...
(e) A prescription prepared in accordance with Sec. 1306.05 written for a Schedule II
narcotic substance to be compounded for the direct administration to a patient by
parenteral, intravenous, intramuscular, subcutaneous or intraspinal infusion may be
transmitted by the practitioner or the practitioner's agent to the pharmacy by facsimile.
The facsimile serves as the original written prescription for purposes of this paragraph
(e) and it shall be maintained in accordance with Sec. 1304.04(h) of this chapter.
(f) A prescription prepared in accordance with Sec. 1306.05 written for Schedule II
substance for a resident of a Long Term Care Facility may be transmitted by the
practitioner or the practitioner's agent to the dispensing pharmacy by facsimile. The
facsimile serves as the original written prescription for purposes of this paragraph (f)
and it shall be maintained in accordance with Sec. 1304.04(h).
(g) A prescription prepared in accordance with Sec. 1306.05 written for a Schedule II
narcotic substance for a patient residing in a hospice certified by Medicare under Title
XVIII or licensed by the state may be transmitted by the practitioner or the
practitioner's agent to the dispensing pharmacy by facsimile. The practitioner or the
practitioner's agent will note on the prescription that the patient is a hospice patient.
The facsimile serves as the original written prescription for purposes of this paragraph
(g) and it shall be maintained in accordance with Sec. 1304.04(h) of this chapter.
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- CAN I MAIL PRESCRIPTION MEDICATIONS CONTAINING NARCOTICS OR
OTHER CONTROLLED SUBSTANCES?
Yes, according to the United States Postal Service regulations.
If the prescription medications have been dispensed in accordance with federal and state
regulations, including proper labeling, and placed in a plain outer container or securely
overwrapped in plain paper which is free of marking that would indicate the nature of the
contents
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- WHERE CAN I FIND A CHART SHOWING THE
DAILY LIMITS FOR RETAIL PSEUDOEPHEDRINE SALES?
The July 2006 Board
newsletter as this article explaining pseudoephedrine sales in
Minnesota.
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- I ALLOWED MY LICENSE TO PRACTICE PHARMACY IN
MINNESOTA TO LAPSE AND NOW I WANT IT REINSTATED. WHAT DO I NEED TO DO?
- In the state of Minnesota a pharmacist is eligible to reinstate their license within two years from the expiration date of the last
time they renewed their license by simply paying back renewal fees, late fees, and
doing their back continuing education.
If they are reinstating after the two year period they need to do the
following.
-
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- DOES YOUR BOARD HAVE LICENSE VERIFICATION ON THE
INTERNET?
Yes, the link can be found here.
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- DOES YOUR BOARD
OF PHARMACY LICENSE OR REGISTER MEDICAL DEVICE OR
MEDICAL SUPPLY MANUFACTURERS, WHOLESALE DISTRIBUTORS, SUPPLIERS OR
RETAILERS?
The Board does not license or register companies that exclusively
manufacture, distribute, supply or sell medical devices or supplies. If a
company that handles medical devices or supplies also manufactures or
distributes drugs, it must be licensed as a drug manufacturer or drug
wholesaler. Exception – if the drug is coated on or embedded in the device
(e.g. drug-coated stents) and the resultant product is approved by the FDA
as a device, the company does not have to be licensed as a manufacturer or
wholesale distributor.
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- WHERE CAN I FIND OUT INFORMATION ABOUT THE BOARD'S CONTINUING EDUCATION REQUIREMENT FOR PHARMACY TECHNICIANS?
The information can be found here.
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contain errors. We present this page to you with a good-faith representation that the
information it contains is generally reliable. Information on this site should not be
relied upon for legal purposes. If you need further information, we encourage you to
contact us directly (651-201-2825) or seek the advice of a professional.
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