NM MPJE QUESTIONS & ANSWERS
What department is the BOP in?
Regulation and Licensing Department
The partially filled DEA 222 CII order must be filled within ___ days from the date of
issuance. The order form is no longer valid after this time.
60
If any person knows or suspects that a licensee is impaired, that person shall report any
relevant information either to the ____ or to the ____.
Impaired Pharmacist Program
Board of Pharmacy
Prior to dispensing any prescription, a pharmacist shall review the patient profile for the
purpose of identifying what 8 things?
(a). clinical abuse/misuse
(b). therapeutic duplication
(c). drug-disease contraindications
(d). drug-drug interactions
(e). incorrect drug dosage
(f). incorrect duration of drug treatment
(g). drug-allergy interactions
(h). appropriate medication indication.
Patient Medication Packages with only one drug within a container stored in a non-
institutional setting may be returned to stock. T or F
false, there is no assurance of storage standards
Patient medication packages with
more than one drug within a container may not under any circumstances be returned to
a pharmacy stock. T or F
true
NM Drug, Device, and Cosmetic Act prevents what 3 things?
,adulteration
misbranding
counterfeiting
The NM, drug, device and cosmetic act's major purpose is to protect the public by
ensuring that drugs, devices, and cosmetics are:
-not ______
-contain proper _____
-not ____ in a ____ way
-properly ____ and ____
-not contaminated
-contain proper ingredients
-not advertised/sold in a misleading way
-properly prescribed and labeled
When a pharmacy is ordering CIIs, who does each copy (1, 2, and 3) of a DEA 222 form
go to?
The purchaser completes the form and submits the Copy 1 and Copy 2 of the form to
the supplier, and retains Copy 3 for his/her own record.
After the supplier gets copy 1 and 2 of the DEA 222 form from the purchaser
(pharmacy), what do they do with these copies?
The supplier must retain Copy 1 of the DEA Form 222 for his or her files and forward
Copy 2 to the DEA agent in the area in which the supplier is located. Copy 2 must be
forwarded at the close of the month during which the order is filled
Tyenol with codeine ≤ ___ per 100mL or ≤ ___ per dosage unit is classified as a CIII.
1.8grams (>200mg)
90mg
Tyenol with codeine ≤ ___ per 100mL or 100grams is classified as a CV.
200mg
morphine ≤ ___ per 100mL or 100 grams with one
or more active, nonnarcotic ingredients in recognized therapeutic amounts is considered
a CIII.
50mg
seco/pento/amo - barbital (barbiturate depressants) mixed with noncontrolled active
ingredient or in suppository dosage form CS class
,CIII
GHB (gamma hydroxybutyrate) CS schedule
CI
anabolic steroids (any drug or hormonal substance,
chemically and pharmacologically related to testosterone) CS schedule
CIII
buprenorphine CS schedule
CIII
ketamine CS schedule
CIII
butalbital + aspirin CS class
CIII
seco/pento/amo - barbital (barbiturate depressants)
CII
dronabinol CS schedule
CIII
benzos CS schedule
CIV
Chlordiazepoxide CS schedule
CIV
phenobarbital CS schedule
CIV
phentermine CS schedule
CIV
modafinil CS schedule
, CIV
Carisoprodol CS schedule
CIV
tramadol CS schedule
CIV
Zaleplon, Zolpidem, Eszopiclone CS schedule
CIV
pregabalin CS schedule
CV
lacosamide CS schedule
CV
lomotil (diphenoxylate/atropine) CS schedule
CV (it's the diphenoxylate that's controlled just FYI)
Schedule of 3,4-methylenedioxymethamphetamine
C-I (ecstasy)
"ISO 5" means air containing no more than ___ particles per cubic foot of air of a size at
least 0.5
micron or larger in diameter
"ISO 5" means air containing no more than 100 particles per cubic foot of air of a size at
least 0.5
micron or larger in diameter
"ISO 7" means air containing no more than ____ particles per cubic foot of air of a size
at least
0.5 micron or larger in diameter
"ISO 7" means air containing no more than 10,000 particles per cubic foot of air of a
size at least
0.5 micron or larger in diameter
What department is the BOP in?
Regulation and Licensing Department
The partially filled DEA 222 CII order must be filled within ___ days from the date of
issuance. The order form is no longer valid after this time.
60
If any person knows or suspects that a licensee is impaired, that person shall report any
relevant information either to the ____ or to the ____.
Impaired Pharmacist Program
Board of Pharmacy
Prior to dispensing any prescription, a pharmacist shall review the patient profile for the
purpose of identifying what 8 things?
(a). clinical abuse/misuse
(b). therapeutic duplication
(c). drug-disease contraindications
(d). drug-drug interactions
(e). incorrect drug dosage
(f). incorrect duration of drug treatment
(g). drug-allergy interactions
(h). appropriate medication indication.
Patient Medication Packages with only one drug within a container stored in a non-
institutional setting may be returned to stock. T or F
false, there is no assurance of storage standards
Patient medication packages with
more than one drug within a container may not under any circumstances be returned to
a pharmacy stock. T or F
true
NM Drug, Device, and Cosmetic Act prevents what 3 things?
,adulteration
misbranding
counterfeiting
The NM, drug, device and cosmetic act's major purpose is to protect the public by
ensuring that drugs, devices, and cosmetics are:
-not ______
-contain proper _____
-not ____ in a ____ way
-properly ____ and ____
-not contaminated
-contain proper ingredients
-not advertised/sold in a misleading way
-properly prescribed and labeled
When a pharmacy is ordering CIIs, who does each copy (1, 2, and 3) of a DEA 222 form
go to?
The purchaser completes the form and submits the Copy 1 and Copy 2 of the form to
the supplier, and retains Copy 3 for his/her own record.
After the supplier gets copy 1 and 2 of the DEA 222 form from the purchaser
(pharmacy), what do they do with these copies?
The supplier must retain Copy 1 of the DEA Form 222 for his or her files and forward
Copy 2 to the DEA agent in the area in which the supplier is located. Copy 2 must be
forwarded at the close of the month during which the order is filled
Tyenol with codeine ≤ ___ per 100mL or ≤ ___ per dosage unit is classified as a CIII.
1.8grams (>200mg)
90mg
Tyenol with codeine ≤ ___ per 100mL or 100grams is classified as a CV.
200mg
morphine ≤ ___ per 100mL or 100 grams with one
or more active, nonnarcotic ingredients in recognized therapeutic amounts is considered
a CIII.
50mg
seco/pento/amo - barbital (barbiturate depressants) mixed with noncontrolled active
ingredient or in suppository dosage form CS class
,CIII
GHB (gamma hydroxybutyrate) CS schedule
CI
anabolic steroids (any drug or hormonal substance,
chemically and pharmacologically related to testosterone) CS schedule
CIII
buprenorphine CS schedule
CIII
ketamine CS schedule
CIII
butalbital + aspirin CS class
CIII
seco/pento/amo - barbital (barbiturate depressants)
CII
dronabinol CS schedule
CIII
benzos CS schedule
CIV
Chlordiazepoxide CS schedule
CIV
phenobarbital CS schedule
CIV
phentermine CS schedule
CIV
modafinil CS schedule
, CIV
Carisoprodol CS schedule
CIV
tramadol CS schedule
CIV
Zaleplon, Zolpidem, Eszopiclone CS schedule
CIV
pregabalin CS schedule
CV
lacosamide CS schedule
CV
lomotil (diphenoxylate/atropine) CS schedule
CV (it's the diphenoxylate that's controlled just FYI)
Schedule of 3,4-methylenedioxymethamphetamine
C-I (ecstasy)
"ISO 5" means air containing no more than ___ particles per cubic foot of air of a size at
least 0.5
micron or larger in diameter
"ISO 5" means air containing no more than 100 particles per cubic foot of air of a size at
least 0.5
micron or larger in diameter
"ISO 7" means air containing no more than ____ particles per cubic foot of air of a size
at least
0.5 micron or larger in diameter
"ISO 7" means air containing no more than 10,000 particles per cubic foot of air of a
size at least
0.5 micron or larger in diameter
