Federal Pharmacy Law Exam 3 Flashcards

The CSA established what kind of system for manufacturing,
distributing, and dispensing controlled substances?

Closed system

Who does an entity have to be registered with to legally engage with
controlled substance activities?

DEA (Drug Enforcement Agency)

The DEA administers and enforces which law?

CSA

The DEA coordinates in conjunction with which organization?

FDA

If a routine pharmacy investigation reveals a controlled substance
violation, then WHO will inform the DEA?

State Board of Pharmacy

Which controlled substance is natural or synthetic opium, opiate and
any derivative thereof?

Narcotic

The controlled substance that is not associated with synthetic opium
is referred to as what?

Non-narcotic

How many schedules of controlled substances are there?

5

What are the determining factors involved with the classification and
schedule of a controlled substance?

Actual or relative potential for abuse Scientific
evidence of the pharmacological effect (if known) State of
current scientific knowledge regarding the drug History and
current pattern of abuse Scope, duration, and significance
of abuse Risk to the public health Physiological
or psychological dependence liability Whether the substance
is an immediate precursor of a substance that is already listed as a
controlled substance

Which drug schedule has the highest potential for abuse?

Schedule I

Are schedule I controls used in medical use for treatment of diseases/disorders?

No (ex. Herroin, Meth, etc.)

Why are schedule I controlled substances not allowed for treatment?

Lack of acceptable information on safety of use, even under medical supervision

Which drug class has a high potential for abuse and is used for
treatments (the highest control used in treatments)?

Schedule II controlled substance

Abuse of C-II medications can lead to what?

Abuse may lead to severe physical or psychological dependence (highly addictive)

Which class has potential for abuse (but less than that of drugs
listed in Schedules I or II)?

Class III

Which classes currently accept medical use in the treatment of
diseases/disorders in the US?

Class II-V

Abuse may lead to limited physical or limited psychological dependence

Class IV and V

True or False: Manufacturers, distributors, and dispensers of
controlled substances must register with the DEA.

TRUE

Potential for abuse (but less than Schedule III)

Schedule IV

Abuse may lead to moderate or low physical dependence or high
psychological dependence

Schedule III

Individuals acting in the normal course of business or employment may
administer, dispense, and prescribe controlled substances under the
registration of the hospital or the institution provided that the:

Hospital or institution has verified that the practitioner is
permitted to dispense, administer, or prescribe within the
jurisdiction Hospital or institution authorizes the
practitioner to dispense, administer, or prescribe under the
hospital registration and designates a specific internal code for
each practitioner Hospital or institution has a current
list of internal codes and corresponding practitioners and is made
available at all times to other registrants and law enforcement
agencies for verification of prescribing authority

Which DEA form is associated with the "Dispenser"?

224

Which DEA form is associated with the "Narcotic Treatment Program"?

363

Which DEA form is associated with "Manufacturer, Distributor,
Importer, Exporter, or Researcher"?

225

With notice to the DEA, registration may be modified under what circumstances?

name or address change

With notice to the DEA, registration may be transferred under what circumstances?

registrant dies, legal existence ceases, professional practice
discontinues, or business is sold

With notice to the DEA, registration may be terminated under what circumstances?

registrant dies, legal existence ceases, or professional practice discontinues

Each registrant is issued a unique registration number by the DEA
known as what?

DEA number

A DEA Number is a 9-character code consisting of what?

2 letters and 7 digits

First character of a DEA number for physicians is what?

A B F

First character of a DEA number for mid-level practitioners is what?

M

First character of a DEA number for distributors is what?

P R

The second character is usually, BUT NOT ALWAYS what?

the first letter of the registrant�s last name

DEA numbers can be verified for accuracy and legitimacy (list these
steps in doing so)

Step 1: Add 1st, 3rd, and 5th digits Step 2: Add 2nd,
4th, and 6th digits and multiply times 2 Step 3: Add Step 1
total and Step 2 total ... the right most digit of this step should
MATCH the 9th character (if not, the DEA number is fake/false)

Do pharmacists have to register for a DEA if they are employed by a
registered pharmacy or institution?

No

A DEA registration is not required for who?

An agent or employee of any registered manufacturer,
distributor, or dispenser if acting in the usual course of business
or employment Common or contract carrier (or employee of),
whose possession of the controlled substance is in the usual course
of business or employment Ultimate user of controlled
substance drug(s) who possesses the controlled substances for a
lawful purpose (i.e. the patient)

What is required for each sale or transfer of a Schedule I or II
controlled substance

DEA form 222

Copy 1 is what color?

Brown

Copy 2 is what color?

Green

Copy 1 and 2 are submitted to whom?

Supplier

The supplier keeps WHAT copy and sends WHAT copy to the DEA

Keeps Copy 1; Sends Copy 2

Copy 3 is what color?

Blue

Copy 3 is kept by whom?

Purchaser

Who can fulfill an order of a 222 form?

registered manufacturers or distributors

If an order cannot be completely filled by the supplier, it may be
partially filled and the balance supplied by additional shipments
within how many days of the original order

60

DEA 222 Forms cannot be filled if they are:

Incomplete, illegible, or not properly prepared, executed or
endorsed Altered (erasure or changed in any manner)

Can a 222 form be corrected if it is not correct the first submission?

No; a new order form must replace it.

If an order is not filled for any reason, the supplier must do what?

Return copies 1 & 2 with an explanation

When received by the purchaser, Copies 1 and 2 (along with the
explanatory statement) must be what?

Attached to copy 3 and retained in the purchaser's files

What must be written on the incorrect 222 form when filed?

VOID

When any line items are canceled by the supplier, the cancellation
must be noted on Copies 1 and 2 how?

By drawing a line through the item

What is written in the space provided for the number of items shipped
if a cancelation of an order occurs?

Canceled

Loss of any used or unused order forms by any purchaser or supplier
must be reported when to the DEA?

Immediately

If an order goes unfilled because the DEA 222 form is lost, the
purchaser must do what?

Complete another form

Purchaser must prepare a statement with the WHAT that indicates the
drugs ordered by the first order form were not received because the
order form was lost

serial number and date of the lost form

Copy 3 of the �second� order form and a copy of the �lost� statement
must be kept with what?

Copy 3 of the �first� order form

Copy of the �lost� statement must be attached to WHAT when sent to
the supplier

Copies 1 and 2

If the �first� order form is subsequently received, the supplier must
write WHAT on the face of the form and return Copies 1 and 2 to the
purchaser who must attach it to Copy 3

Not accepted�

What is the electronic equivalent to the DEA 222?

CSOS

Advantages of using CSOS:

Greater ordering freedom � no maximum number of line items
Faster transactions � electronic �certificate� contains the same
identification information as the DEA Form 222 which allows for
timely and accurate validation by the supplier Accurate
orders � reduces the number of ordering errors Decreased
cost � greater accuracy and decreased paperwork = lower transaction
costs

Registrants who purchase controlled substances for the purpose of
repackaging � either for the sale within the pharmacy or to other
registrants - must register as a

Manufacturer

Pharmacy may compound a controlled substance for �office use� so long
as the product:

is an aqueous, oleaginous, or solid dosage form does
not contain >20% of a controlled substance is only
distributed to a practitioner who is authorized to dispense

Practitioners must be separately registered with the DEA to
administer or dispense narcotic drugs (in any schedule) to a narcotic
drug-dependent person for what?

�detoxification treatment� or �maintenance treatment�

Physicians who are not separately registered with the DEA may
administer narcotics for the relief of WHAT while arrangements are
made for appropriate treatment?

acute withdrawal

What is the day supply that not registered physicians can supply for
acute withdrawal of patients?

One day

How many days can a physician not registered prescribe a narcotic for
acute relief?

3 days (each one day supplies at a time)

ALL controlled substance prescriptions MUST be signed and dated on
the day written and must include:

Full name and address of the patient Drug name,
strength, and dosage form Quantity prescribed
Directions for use Name, address, and DEA number of the
prescriber NPI number of prescriber

True or False: The prescriber's signature can be written in pencil

False; must be indelible (cannot be erased)

Can nurses sign for doctor's when issuing a controlled substance prescription?

No; they can prepare the script, but it is the doctor's
responsibility to sign

Prescribers must use a WHAT to electronically sign the prescription
which serves as the legal signature of the prescriber

two-factor credential

A paper copy of an electronic prescription may be given to the
patient if it is clearly labeled with:

COPY ONLY - NOT VALID FOR DISPENSING�

A �back up� of electronic prescriptions must be completed daily and
kept for how long?

2 years

A �back up� of electronic prescriptions must be completed daily and
are kept for how long (in accordance to the MMA)

10 years

If duplicate e-prescriptions are received, the pharmacist must do what?

Mark one "VOID

If a paper or oral prescription indicates the original prescription
was transmitted electronically to another pharmacy, the pharmacist
must do what?

Check with the other pharmacy to determine if the e-script was
received and dispensed

If the e-prescription was received but NOT dispensed, the other
pharmacy must do what?

mark the e-prescription �VOID�

If the e-prescription was received AND dispensed, the pharmacy
presented with the paper/oral prescription MAY NOT dispense the drug
and MUST do what?

mark the paper/oral prescription �VOID�

True/False: Practitioners may issue prescriptions for multiple
patients with a single signature

FALSE

True/False: Practitioners may sign multiple prescriptions for a
SINGLE patient at one time

TRUE

Can a prescription be post dated?

No

True/False: Once an e-prescription has been signed by the prescriber,
it does not have to be transmitted to the pharmacy immediately

TRUE

True/False: In the event that an e-prescription fails to �send�, it
may be converted by an intermediary to another electronic form

False: May not be converted

If an e-script fails to send for a control a physician must take what action?

Physically print the Rx, manually sign it, and fax it to pharmacy
directly, and it must be documented on the script that the electronic
transmission failed

A pharmacist may dispense a CII medication pursuant to a WHAT prescription

signed,written

When can a pharmacist take an oral prescription for a C-II?

In an emergency situation

What is considered an "emergency situation" when dispensing
a C-II?

Immediate administration is necessary for proper treatment
No appropriate alternative plan is available Not
reasonably possible for the prescriber to provide a written
prescription to the patient before dispensing

True or False: A practitioner may administer or dispense a CII
medication in the course of professional practice without a
prescription for maintenance or detoxification treatment if
requirements are met

TRUE

A WHAT may administer or dispense a CII medication upon receipt of a
written prescription or an order to be dispensed for immediate
administration to the ultimate user

institutional practitioner

A pharmacist may dispense a CII medication in an emergency situation
under what specifics?

Immediate administration is necessary for proper treatment
No appropriate alternative plan is available Not
reasonably possible for the prescriber to provide a written
prescription to the patient before dispensing

Quantity prescribed and dispensed must be limited to an amount
adequate for how long in an emergency C-II prescription fill?

the emergency period ONLY

In an emergency C-II fill the prescription must be immediately
reduced in writing by the pharmacist and must contain all required
information for a written CII prescription except for what?

The prescribers signature

When must a cover prescription be provided from the physician in an
emergency fill situation?

Within 7 days

What must be explicitly written on an emergency C-II prescription?

'Authorization for Emergency Dispensing�

The pharmacist notifies whom if a cover script is not provided within
7 days from the prescriber?

DEA

The pharmacist must make every reasonable effort to verify what when
filling an emergency C-II medication?

The prescriber's identity

WHICH pharmacies MAY NOT prepare CII prescriptions for dispensing
from oral authorization

Central fill

CII prescriptions may be faxed to the dispensing pharmacy and can
serve as the original written prescription if:

A home infusion pharmacy receives the prescriptions for
parenteral administration A resident of a Long Term Care
Facility (LTCF) is the intended recipient of the prescription
A patient enrolled in hospice is the intended recipient of the
prescription

In GA what must be written on the script for Hospice faxed CII?

HOSPICE

In GA what must be written on the script for Long Term Care Facility
faxed CII?

LTCF

Faxing a CII prescription to the dispensing pharmacy for any other
reason is for what only?

Informational purposes

Can a faxed CII that is not from Hospice or LTCF be filled?

No, there must be an original prescription provided

Pharmacists are NEVER allowed to change what on a CII?

The patient�s name The medication prescribed
The prescriber�s signature

In Georgia, pharmacists may �add� or �change� what on a CII?

quantity prescribed and/or the medication strength

Changes on a CII must result in what action by the pharmacist?

Changes noted on face of prescription Pharmacists
initials

Additionally, a pharmacist needs to do what when editing a CII?

Documenting date and time and brief explanation of conversation with prescriber

Can a CII be refilled?

No

Partial filling of a CII is permitted when?

The pharmacist is unable to supply the full quantity due to
lack of inventory The patient is in a LTCF or has a
�terminal illness�

When partial filling a script due to lack of inventory, the quantity
dispensed must be noted on the face of the prescription and the
remaining portion must be filled within

72 hours

If the remaining portion cannot be supplied in 72 hours, the
pharmacist must do what?

Notify prescribers for a new prescription

What must be recorded with each partial fill in an LTCF

The quantity dispensed date remaining
quantity authorized for dispensing the pharmacist�s
identification

The prescription is valid for partial filling for up to how long from
the date of issuance

60 days

The total quantity dispensed in partial filling cannot exceed what?

the total quantity originally prescribed

A community pharmacist may dispense a Schedule III, IV or V
medication pursuant to:

A written prescription signed by a prescriber A fax of
a written prescription transmitted by the prescriber An
electronic prescription meeting CSA requirements An oral
prescription that is promptly reduced in writing by the
pharmacist

An institutional pharmacist may administer or dispense a Schedule
III, IV or V medication pursuant to:

A written prescription signed by a prescriber A fax of
a written prescription or order transmitted by the prescriber
An electronic prescription meeting CSA requirements An
oral prescription that is promptly reduced in writing by the
pharmacist An order by a prescriber that is dispensed for
immediate administration

True/False: A prescriber may administer or dispense a CIII, CIV, or
CV directly to a patient in the course of professional practice
without a prescription

TRUE

CIII and CIV controlled substance prescriptions MAY NOT be refilled
more than how many times in a 6 month period from the date of issuance
nor can fills exceed the number of refills permitted, if any were
originally allowed by the prescriber

5 times

CV prescription refills must be in accordance with what?

prescriber allowances state regulations

In GA...CV controlled substance prescriptions follow same rules as
what other classes?

CIII and CIV

A record of each refill must be kept and must include:

Name and dosage form of the medication dispensed Date
filled Quantity dispensed Initials of dispensing
pharmacist Total number of refills remaining, if any, for the
prescription

The prescriber may orally authorize additional refills for a CIII or
CIV prescription if:

The total quantity authorized, including original amount, does
not exceed 5 refills in a 6 month period The quantity of
each additional refill is equal to or less than the original
quantity prescribed?

The pharmacist obtaining oral authorization must record the following
on the original paper prescription:

Date of authorization Quantity permitted per
refill Number of additional refills authorized
Initials of the pharmacist who received the authorization

The prescriber must issue a �new� prescription for any quantity
beyond what?

5 refills, or 6 months

Pharmacies may use ONE OF TWO record-keeping systems:

Paper record-keeping system (back of the original
prescription) Computerized record-keeping system

Paper system, the pharmacist must record on the original paper prescription:

Date of authorization Quantity permitted per
refill Number of additional refills authorized
Initials of the pharmacist who received the authorization

WHAT must provide on-line retrieval of original prescriptions
currently authorized for refilling and the refill history

Computerized system

WHAT of each day�s controlled substance refill data must be verified,
dated, and signed the pharmacist

Hard-copy printout (log)

Partial filling is allowed provided that:

Each partial fill is recorded in the same manner as a
refill Total quantity dispensed in all partial fillings does
not exceed the total quantity prescribed Dispensing does
not occur 6 months beyond the date the prescription was issued

Which substance that IS NOT a prescription medication pursuant to
federal, state, or local law may be dispensed by a pharmacist without
a prescription

CV

The dispensing of a CV may only be done by whom?

The pharmacist

True/False: A CV must be sold by a pharmacist

False: Can be sold by other employees

The quantity dispensed of a CV in a 48-hour period is not more than:

240mL or 48-dosage units of an opium containing substance
120mL or 24-dosage units of any other controlled substance

A purchaser of a CV must be what age?

18 (ID Required)

A controlled substance log book must be maintained for how long by a pharmacist?

2 years

The controlled substance log book must contain what?

Name and address of purchaser Name and quantity of
controlled substance purchased Date of purchase
Name or initials of dispensing pharmacist

In Georgia ... a pharmacist may sell or dispense up to how much of an
exempted, non-pseudoephedrine Schedule V substance in a 48-hour period?

4 ounces or 32 dosage units

In GA, what are the requirements of dispensing a CV?

The pharmacist has applied reasonable means to determine that
the product is being used for a legitimate medical purpose
The purchaser has completed all controlled substance �log� book
requirements

A controlled prescription label must contain:

Date of fill Pharmacy name and address Serial
number of the prescription Name of patient?Name of
prescriber Directions for use?Warning statement �Caution:
Federal law prohibits the transfer...� Other cautionary
statements, if needed or required by law

In GA... a controlled prescription label must include the federal
labeling requirements PLUS:

Telephone number of dispensing pharmacy Date of
initial fill or refill Drug expiration date, if any

Which Schedule II prescription labels ARE NOT required to contain the
same information

Institutional

INSTITUTIONAL Schedule II prescription labels ARE NOTrequired to
contain the same information provided that:

< 7-day supply is dispensed a one time The
medication is NOT in the possession of the user prior to
administration The institution maintains appropriate records
related to administration, control, dispensing, and storage
The system used by the pharmacist to fill the prescription can
identify the supplier, product, patient, directions for use, and
cautionary statements

INSTITUTIONAL Schedule III, IV or V prescription labels ARE NOT
required to contain the same information provided that:

< 34-day supply or 100 dosage units dispensed at one
time The medication is NOT in the possession of the user
prior to administration The institution maintains
appropriate records related to administration, control, dispensing,
and storage The system used by the pharmacist to fill the
prescription can identify the supplier, product, directions for use,
and cautionary statements

Original prescription information for Schedule III, IV, or V
medications may be transferred how many times between pharmacies for
refill purposes?

one-time

Pharmacies electronically sharing a WHAT may transfer Schedule III,
IV, or V Rx information up to the maximum number of refills permitted

a real-time, online database

All transfers must be communicated directly between whom?

2 licensed pharmacists

The original and transferred prescription records must be maintained
for how long from the date of the last refill

2 years

�Transferring pharmacist� must:

Invalidate the original prescription Record name,
address, DEA registration number, and name of �receiving
pharmacy/pharmacist� Record the date of transfer and the name
of �transferring pharmacy/pharmacist�

How does a transferring pharmacist invalidate the original prescription?

Write �Void� on the face of the original paper
prescription Transfer data/information must be added to the
electronic prescription record

The recorded name, address, DEA registration number, and name of
�receiving pharmacy/pharmacist� and the recorded the date of transfer
and the name of �transferring pharmacy/pharmacist� is done how?

Must be recorded on the back of the invalidated paper
prescription Information must be documented in the electronic
prescription record

�Receiving pharmacist� must:

Write �TRANSFER� on the face of the prescription Enter
all information required by the CSA for prescriptions

Enter all information required by the CSA for prescriptions means the
receiving pharmacist must do what?

Date the original prescription was written and dispensed
Original number of refills and number of valid refills
remaining Date and location of previous refill(s)
Pharmacy�s name, address, DEA registration number, and
prescription number from which the prescription information was
transferred Name of the �transferring pharmacist�

Once the receiving pharmacist follows the correct procedures, what
must be done?

An electronic prescription record must then be created

Schedule III, IV, or V prescriptions may be transmitted
electronically or by fax from a retail pharmacy to a

central fill pharmacy

Retail pharmacy transmitting the prescription to a central fill
pharmacy must:

Write �CENTRAL FILL� on the face of the original
prescription Record the name, address, and DEA registration
number of the central fill pharmacy Record the date of the
transmission to the central fill pharmacy Indicate the
number of refills already dispensed and the number of refills
remaining Maintain original prescription for 2 years from the
date of the last refill Keep a record of receipt of the
filled prescription (date, method of delivery, and name of retail
employee accepting delivery)

Central fill pharmacy receiving the prescription must:

Keep a copy of the faxed prescription or an electronic record
of all information transmitted by the retail pharmacy
Record the date of receipt of the transmitted prescription, name
of filling RPh, and filling/refill dates Record the date
the filled prescription was delivered to and the method of delivery
to the retail pharmacy

THESE are registered with the DEA for controlled substance disposal
and/or destruction

Reverse distributor

For disposal or destruction of Schedule II medications a reverse
distributor must do what?

Issue a DEA Form 222 or its electronic equivalent to the pharmacy

For disposal or destruction of Schedule III, IV, or V medications:

The pharmacy maintains a record of the drug name, dosage form,
strength, quantity, and date transferred

A reverse distributor submits which form to the DEA when destruction
is complete

DEA form 41

Registered pharmacies may distribute and/or transfer �a quantity for
general dispensing� of controlled substances between each other
provided that:

The distribution is recorded by the distributing and receiving
pharmacy A DEA Form 222 is used if Schedule II medications
are involved The total number of dosage units of all
controlled substances distributed or transferred in a calendar year
DOES NOT exceed 5% of the total number of dosage units distributed
and dispensed in the same calendar year

f the quantity is >5%, the business must register as a what?

Distributor

True or False: Prescribers ARE required to keep records of Schedule
II, III, IV, and V medications that are prescribedin the normal course
of their practice unless it is a part of a maintenance or
detoxification program

False: They are NOT REQUIRED to keep records

True or False: Prescribers ARE required to keep records of Schedule
II, III, IV, and V medications that are dispensed in their practice

TRUE

True or False: Prescribers ARE NOT required to keep records of
Schedule II, III, IV, and V medications administered in their practice
IF they regularly engage in administering controlled substances and if
they charge patients for the service

False; they ARE required

Two file system (Option 1):

Schedule II prescriptions are in a SEPARATE file
Schedule III, IV, and V prescriptions are marked with a one inch
high red �C� stamp and filed with non-controlled substance
prescriptions

Two file system (Option 2):

Schedule II, III, IV, and V prescriptions are filed together?
Schedule III, IV, and V prescriptions are marked with a
one inch high red �C� stamp? Non-controlled
substance prescriptions are in a SEPARATE file

Three file system:

Schedule II prescriptions are in a SEPARATE file
Schedule III, IV, and V prescriptions are in a SEPARATE
file Non-controlled substance prescriptions are in a SEPARATE
file

A controlled substance inventory MUST be taken at least once HOW OFTEN?

Every 2 years (biennial inventory)

Inventory requirements must be kept for how long?

2 years

Inventory records must be maintained in a SEPARATE file from all
other inventory records in regards to what schedule of controls?

I and II

Schedule III, IV, and V inventory records must be maintained in a
SEPARATE file from non-controlled substance inventory records or in a
manner that makes them WHAT from ordinary records

READILY RETRIEVEABLE

Inventory records should be maintained in written, typewritten, or
printed form and signed by whom?

The person conducting the inventory

Controlled substance financial and shipping records may be kept at a
central location provided that the registrant has notified WHOM of the
intent of central record keeping

the DEA

When conducting a controlled substance inventory:

An exact count is required for all sealed, unopened
containers An exact count is required for all Schedule II
opened containers An estimated count is acceptable for
Schedule III, IV or V�s if the package size contains <1000 dosage
units

Those authorized to conduct research or chemical analysis using
controlled substances MUST store Schedule II, III, IV and V
medications in a WHAT?

securely locked, substantially constructed cabinet

Pharmacies may store Schedule II, III, IV and Vmedications by:

Keeping them in a locked, secure cabinet Dispersing
them through the non-controlled substance stock in an effort to
prevent theft or diversion

Which drugs MUST be stored in a safe or steel cabinet that is
equivalent to a US Government Class V security container

Carfentanil etorphine diprenorphine

Significant theft or loss of controlled substances must be reported
to the DEA when?

immediately upon discovery (pilferage, fire, natural disaster, etc.)

The pharmacy must complete which DEA Form to formally document the
quantities and circumstances of the theft or loss

DEA Form 106

In addition to notifying the DEA about the loss of controls, the
pharmacy must inform whom?

Local law enforcement

Who is responsible for reporting (to the DEA) any in-transit loss of
controlled substances

Suppliers

Pharmacies are responsible for reporting (to the DEA) loss after a
pharmacist has WHAT of a medication shipment

signed for or taken custody

If an in-transit loss occurs but it is not discovered until AFTER the
pharmacist has taken custody, then the pharmacist must submit which
DEA Form?

106

The Controlled Substance Registrant Protection Act of 1984 allows for
the federal investigation of thefts and robberies if:

The replacement cost of the controlled substance(s) taken is ?
$500 Someone is killed or suffers �significant bodily injury�
during the commission of the crime Interstate or foreign
commerce is involved in planning or executing the crime

The CMEA limits retail PSE purchasers to what quantity in a day?

less than or equal to 3.6 gm/day

The CMEA limits retail PSE purchasers to what quantity in a 30 day period?

less than or equal to 9 gm/30 day period

The CMEA limits retail PSE purchasers to what quantity in a 30 day
period via mail order?

less than or equal to 7.5 gm/30 day period

Non-liquid forms of PSE must be sold in blister packs with no more
than how many units per pack?

2 dosage units

All PSE products must kept where?

behind the counter (not necessarily the pharmacy counter) or in a
locked display case on the selling floor

Retailers must train applicable sales personnel and submit
self-certifications to whom?

The attorney general

Logbook requirements do not apply to any purchases of �single sale�
packages that contain what quantity of PSE

less than or equal to 60 mg

Electronic logbooks must be maintained of all transactions where the
purchaser records their what?

signature, name, address, date, and time of sale

Logbooks for PSE must be maintained for how many years?

2 years

In GA PSE is considered what?

�exempt Schedule V� controlled substance