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WorksheetsDDS Lab Practice Exam
Total questions: 100
Worksheet time: 54mins
Inert filler to create desired bulk, flow properties, and compression characteristics of tablets and capsules
Diluent
Disintegrant
Anti-adherent
Glidant
Study that concern itself with the physical, chemical and biological factors which influenced the formulation, manufacture, stability and effectiveness of pharmaceutical dosage forms
Pharmaceutics
Pharmacokinetics
Pharmaceuticals
Pharmacology
Generally, pharmaceutics deals with the formulation of new drug substances into the dosage form, from raw or starting materials to the finish product.
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Extemporaneous preparations are compounded by the pharmacists for specific patients because some drugs are readily available in the market
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Function of Pharmaceutical Ingredients EXCEPT
provides bulkiness to the formulation
facilitates absorption of drugs
provides stability
prevent denaturation
NOTA
Contaminants promote bacterial growth. Hence, patient can use contaminated products
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Steps in Compounding EXCEPT
Preparatory
Final Check
Sign-Off
Cleanup
NOTA
Compounding and cleaning is mandatory in clearance
TAMA
MALI
Signing and dating the prescription affirms that all of the indicated procedures were carried out to ensure:
I. uniformity, identity, strength, quantity, purity
II. clean
III. validation from health authority
I and II
III only
I only
II only
Prevent tablet ingredients from sticking to punches and dies during production
antiadherents
binders
diluent
opaquant
Uses of tablet coating agent
protect against decomposition by atmospheric oxygen or humidity
provide a desired release pattern
mask taste or odor
for estetik purposes
A thin cover around a formed tablet or bead
film coating
sugar coating
enteric coating
plastic coating
Used in tablet and capsule formulations to improve flow properties of the powder mixture
Glidant
Diluent
Lubricant
Colorant
Opaquant may be used alone or with a colorant in tablet and capsule
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Used to impart an attractive sheen to coated tablets
Polishing agent
Stiffening agent
Encapsulating agent
Levigating agent
Used to form thin shells to enclose a drug for ease of administration. Ex. Gelatin
Encapsulating agent
Polishing agent
Opaquant
Stiffening agent
Used to prevent drying of preparations, particularly ointments and creams
Humectant
Stiffening agent
Buffer
Levigating agent
Used to increase thickness or hardness of a preparation, usually an ointment
Stiffening agent
Buffer
Humectant
Lubricant
Used to resist change in pH upon dilution or addition of acid or alkali
Buffer
Humectant
Glidant
Resister
Substance that forms stable water-soluble complexes (chelates) with metals; used in some liquid pharmaceuticals as stabilizers to complex heavy metals that might promote instability.
Sequestering agents
Chelating agent
Stiffening agent
Polishing agent
Containers according to their ability to protect the contents from external conditions EXCEPT
Hermetic container
Light-resistant
Child-resistant
NOTA
protects the contents from other solids and from loss of the article under normal
WELL-CLOSED
TIGHTLY-CLOSED
HERMETIC
CHILD RESISTANT
It protects the contents from contamination by extraneous liquids, solids or vapors, from loss of the article and from efflorescence
TIGHTLY-CLOSED
WELL-CLOSED
HERMETIC
CHILD RESISTANT
phenomena where the water of crystallization of substance evaporates upon exposure to dry environment
Hydroscopic
Deliquescent
Eutectic
Efflorescence
USP standard on limit if light transmission
290-450nm
100-190nm
190-350nm
990-1000nm
A child resistant container that is significantly difficult for children under 8 years of age to open
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alerts the consumers of foul play or damage to the product
tamper evident
well closed
tightly closed
single dose container
Example of Tamper Evident Containers EXCEPT
Shrink seal band
Sealed carton
Breakable cap
Well-closed
Parenteral preparation does not require to meet the antimicrobial effectiveness requirement because it is for single dose only
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EXAMPLES OF SINGLE DOSE CONTAINER EXCEPT
Ampules
Prefilled syringes or cartidges
Blister pack
Vials
Multiple dose container usually expires in 28 days when opened unless there is indication in the container
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Parenteral products only EXCEPT
highly-resistant borosiicate glass
treated soda-lime glass
soda-lime glass
general purpose soda-lime glass
rigid and has good clarity; useful in blister packaging of
tablets and capsules. Not suitable when gamma sterilization is required
PVC
PET
APET
PETG
____ and _____ have excellent transparency and luster can be sterilized with gamma radiation
APET, PETG
PVC, PET
PET, PETG
PVC, PETG
Plastic squeeze bottles are common in ophthalmic and otic preparations
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Used for dispensing liquids of low viscosity
Rx bottle
Round bottle
Wide mouth bottle
Collapsible tube
According to federal regulations, manufacturers' drug product labeling includes:
labels on the immediate container and packaging but also inserts
company literature; advertising and promotional material
computer-accessed information
price lists
Label of Supplement Facts includes:
Statement of Identity
Name of Dietary Supplement
Nutrition value
Name and place of manufacturer, packer and distributor
USP product standardization program is mandatory participation
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Maybe
Sometimes true, sometimes false
STORAGE CONDITIONS: COLD
not exceeding 8 C
between 8-15 C
temp prevailing in working place
15-30 C
STORAGE CONDITIONS: COOL
not exceeding 8 C
8-15 C
25 C
NOTA
Tablets and Capsules shelf life is minimum of 5 years the date of preparation
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example of oral use EXCEPT
sublingual
buccal
perlingual
per-oral
What is the DOSAGE STRENGTH of Dantrolene Syrup per 6 mL?
Dantrolene .............................. 625 mg
Citric acid ................................. 150 mg
Simple syrup ........................... 10 mL
Purified water qs ad .............. 125 mL
(a)
What is the quantity of Citric Acid, if formulation is adjusted to make 500 mL?
Dantrolene .............................. 625 mg
Citric acid ................................. 150 mg
Simple syrup ........................... 10 mL
Purified water qs ad .............. 125 mL
(a)
What is the quantity of Dantrolene Sodium (IN GRAMS), if the formulation is adjusted to make 450mL?
Dantrolene .............................. 625 mg
Citric acid ................................. 150 mg
Simple syrup ........................... 10 mL
Purified water qs ad .............. 125 mL
(a)
Nitrogylcerin tablet triturate is intended to be dissolved or taken in the buccal pouch.
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Used by doctors in extemporaneous preparation of parenteral solutions
Hypodermic tablets
Enteric-coated tablets
Sugar coated tablets
Pills
Molded tablets are generally prepared by mixing the active drug with lactose, dextrose, sucrose, mannitol, or some other appropriate diluent that can serve as the base.
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SYNONYMS OF TABLET TRITURATES
Molded tablets
Tabella triturate
Tableta trituratii
Tableta quadturatii
less than 20 mg (potent substance with cooling agents)
Parvules (small pills)
Granules
Pills
Boluses (big pills)
20 mg to 60 mg (contains sugar)
Granules
Parvules
Pills
Boluses
The standard moisture content specification for hard gelatin capsules.
13-16% w/w
15-26% w/w
10-16% w/w
10%
Clindamycin hydrochloride
Dalasinsing
Folart
Advil
Medicol
gelatin derived from pork skin by acid processing
Type A
Type B
Type AB
Type O
gelatin obtained from bones and animal skins by alkaline processing
Type A
Type B
Type AB
Type O
sifting is acceptable for theincorporation of potent drugs into a diluent powder
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- Moisture-activated adherent
- An ethylene oxide polymer with a high molecular weight
- Forms a viscous, mucoadhesive gel
Polyox
Aquaphor
Erythrosine
Iron oxide
Commercial antibiotic products
BIAXIN (Clarithromycinomnicef)
LACTINEX
IMODIUM
NEOZEP
Commercial probiotic products
BIAXIN (Clarithromycinomnicef)
LACTINEX
IMODIUM
ADVIL
suppository that is globular, oviform and cone shape
Pessaries
Bougies
Rectal for Infant
Rectal for Adult
Migraine
Ergotamine tartrate
Indomethacin
Oxymorphone and morphine
Prochlorperazine andChlorpromazine
NSAID
Indomethacin
Opioid
Oxymorphone
Prochlorperazine
PSYCHOLOGICAL FACTORS EXCEPT
Circulation route
pH of Rectal fluids
Colonic content
lipid- water solubility
PHYSIOCHEMICAL FACTORS EXCEPT
Lipid- water solubility
Particle size
Nature of base
Colonic content
Rectal fluids are not essentially neutral in pH andhave effective buffer capacity.
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- triglycerides of saturated fatty acids
- came from lauric acid
WITEPSOL BASES
WECOBEE BASES
FATTIBASE®
COCOA BUTTER BASE
STIFFENING AGENT FOR GLYCERIN SUPP
SODIUM CARBONATE & STEARIC ACID
SODIUM CARBONATE & CITRIC ACID
SODIUM CARBONATE & TARTARIC ACID
NOTA
When tartaric acid (only) is added to Na phosphate effervescent granules, powder will be crumble and if citric acid only, it will result to sticky
TAMA
MALI
DRY OR FUSION METHOD: The ____ acts as the binding agent
water of crystallization of citric acid
water
alcohol
citric acid
Synonyms of ointments
SALVE
CHRISMA
UNGUENTUM
OINTION
Moistening agent in the preparation of tablet
Water
95% zinc oxide
95% Ethyl alcohol
H2O
This is added in soft gelatin capsule formation to ensure adequate flexibility
Plasticizing agent
lubricant
Lactose
Disintegrant
- most ingredients used in ointment bases will liquefy around __ degree Celsius
70
100
80
17
Accelerate the cooling process by putting the melt in water or ice. This will not change the consistency of the final product making it more viscous than desired.
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Uses fusion method EXCEPT
Zinc ointment
Coal Tar Ointment
Anthralin Ointment
Yellow Ointment
It is added to reduce the penetration of light into the capsule to protect photosensitive drug
Titanium dioxide
Lactose
Sucrose
Parabens
It is cylindrical in shape and tapered at one end or both forming a bullet shape end.
Rectal supp.
Vaginal supp.
Urethral supp.
wala akong pake
In this process, the powder is pressed between rollers to increase density of a powder.
Dry granulation
Wet granulation
Direct granulation
Fusion method
This method is not applicable for moisture sensitive powders
Wet granulation
Dry granulation
Medyo dry granulation
#NeverAgain
It is the acidifier in the formulation of Sodium Phosphate effervescent granules
Tartaric acid
Citric acid
Sulfuric acid
Mefenamic acid
USES OF ZINC OXIDE PASTE
Astringent
protective
vehicle
Antacid
preservative In cold cream
Sodium borate
mineral oil
Cetyl ester wax
Beeswax
greaseless bases
WATER SOLUBLE BASE
WATER-REMOVABLE BASE
water-washable bases
ABSORPTION BASE
Medicated ointment uses EXCEPT
antiseptic
antibacterial
anti-inflammatory
anti-thrombotic
Stiffening agent of Glycerol suppositories
Glycerin
Sodium carbonate
Stearic acid
Tartaric acid
TYPES OF STABILITY: Physical
Appearance
Sterility
Resistance to microbial growth
No significant increases in toxicity
Dietary products may not have a disclaimer statement
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In this method, the powder is dissolved in volatile solvent. Then the powder re-crystallizes after the solvent evaporates.
Pulverization by intervention
Dry granulation
Wet na wet granulation
Levigation
Official room temperature
25 °C
Not exceeding 8 °C
37 °C
Above 40 °C
used as a preservative in pills and might be omitted if only a small batch of pill mass was being compounded.
Benzoic acid
Citric acid
Tartaric acid
Sulfuric acid
What is the quantity of thioguanine (in mg) needed to compound this oral suspension, if required dose is 20mg/mL?
(a)
best used on dry skin.
ointment
paste
gel
in applying ointment. inunction is required
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Latin name of ZnO paste
Pasta zinci oxide
Pesto zinci oxide
Spaghetti zinci oxide
Latin zinci oxide
vehicle of ZnO paste
White petrolatum
Yellow petrolatum
While ointment
Yellow ointment
Paste: because of their low powder content, they are often used to absorb wound exudates
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used to remove warts, calluses, or other lesions in which the epidermis produces excess skin
Fungicide
Keratolytic
Keratin
Bactericidal
Incorporation of a gummy material via pulverization by intervention
Camphor
Aquaphor
Epsom salt
Magnesii sulfas pillulas
formerly, the pills are the most extensive used oral dosage form, but it is replaced by compressed tablets and capsules
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HA
DI KO GETS
