USP requires tests for capsules that include which of the following? Stability testing, and disintegration testing Added substances and dissolution test Content uniformity and weight variation All of these are required tests so this is the answer

The dissolution of the drug from the dosage unit during the elapsed time is the USP test requirement for which of the following? A. Product uniformity and weight variation B. Drug release for extended release or delayed release dosage forms C. Microencapsulation and fluid bed processing D. Teeth, hair and eyeballs

Which of the following are NOT tablet quality requirements of the USP? (read carefully) A. Disintegration and dissolution tests B. Weight and weight variation tests C. Thickness and hardness tests D. Fryability and bakeability

The following preparations should have the auxillary label, “SHAKE WELL”(1 Point)Milk of MagnesiaLinimentsNystatin suspensionAll of theseNone of theseWhich of the following statements is TRUE regarding capsule shells?I. Depending on their composition, gelatin capsule shells may be hard or softII. The shell may be composed of two pieces, a body and a capIII. The capsule shell may be a single piece that is often referred to as a soft gelatin capsule(1 Point)I and IIIIIIII and IIII, II and IIIWhich statement about training personnel for aseptic compounding is correct?(1 Point)Compounders may either wash hands before compounding or wear sterile gloves.Annual media-fill testing is required at least once per year.Guidelines are described in USP <795>.Training is focused primarily on protecting the compounder during aseptic processing.Which of the following statements is TRUE regarding elixirs?I. Ethanol and water are the main ingredients II. Clear, pleasantly flavored, sweetened hydroalcoholic liquids for oral useIII. These are more fluid than syrups(1 Point)I onlyIII onlyI and IIII and IIII, II, and IIIAll of the following compounding practices are required for radiopharmaceuticals except:(1 Point)must account for transport time in the design.absence of clothing and materials exposed in patient care areas.not less than an ISO Class 7 air environment in the segregated compounding area.single-dose injections of ≤100 mL meet the USP <797> standards for low-risk level CSPs.visual inspection of radioactive CSPs limits personnel exposure to ALARA.

Test performed to compare the weight or volume of a product filled into each container with their labeled weight or volume(1 Point)Water contentMinimum fillStorageall of the thesenone of theseWhich is a common biological indicator for pharmaceutical sterilization processes?(1 Point)B. subtilisC. difficileC. albicansH. influenzaeRecommended packaging of ointments:(1 Point)Collapsible tubestight containerswell-closed containersall of the thesenone of theseWhich of the following types of inert ingredients/substances is prohibited in injections?(1 Point)AntioxidantspH buffersAntimicrobial preservativesColoringsBenzyl alcoholWhich is an advantage of suspensions over solutions for ophthalmic delivery?(1 Point)Suspensions do not cause stinging or burning sensation.Suspensions provide a longer corneal contact time.Suspensions do not require a preservative.One drop of suspension is smaller than one drop of solution.The eye can hold a greater volume of suspension than solution.Which of the following technologies is an example of reverse genetics?(1 Point)Recombinant DNAPolymerase chain reactionGene insertionMurine MAbAntisense RNA

Capsule manufacturing defects that have been resolved by tapering the rim of the capsule body include which of the following? 1. Stratification and segregation 2. Disintegration and dissolution 3. Capping and lamination 4. Splitting and denting