1. Store in a cool place means
A. Store between 8-25 °C
B. between 2-8 °C
C. Any temperature above 40 °C
D. Under protection from moisture, freezing and excessive heat
A. Store between 8-25 °C
B. between 2-8 °C
C. Any temperature above 40 °C
D. Under protection from moisture, freezing and excessive heat
2. Teaspoonful contains
A. 8 ml
B. 10 ml
C. 5 ml
D. 1 ml
3. Schedule C related to
A. Standards for surgical dressings
B. Prescription drugs
C. Biological & special products
D. GMP
4. Class 100 area term is related to
A. Manufacturing area
B. Clean room
C. Ware house
D. Aseptic area
5. The purpose of the seal coating in sugar coating process for tablets is used
A. To prevent moisture penetration into the tablet core
B. To round the edges and build up the tablet weight
C. To impart the desired colour to the tablet
D. To give lustre to the tablet
6. Progesterone injection BP is a sterile solution in
A. Water
B. Ethyloleate
C. Propylene glycol
D. Glycerol
7. If the carr’s index of a powder is 10% then the type of powder flow is
A. Poor
B. Excellent
C. Very poor
D. Good
8. Table spoonful measures
A. 5 ml
B. 8 ml
C. 15 ml
D. 30 ml
9. The disintegration time for sugar coated tablet is
A. 30 minutes
B. 45 minutes
C. 60 minutes
D. 75 minutes
10. Liquid paraffin exhibits
A. Plastic flow
B. Newtonian flow
C. Pseudoplastic flow
D. Dilatants flow
11. Disintegration time for hard gelatin capsule as per IP
A. 15 min
B. 30 min
C. 60 min
D. 75 min
12. Schedule S deals with
A. Standards for disinfectant fluids
B. Drugs which are habit forming
C. Standards for ophthalmic preparation
D. Standards for cosmetics.
13. In the preparation of multilayer tablets one of the substances listed is for Hydrophilic matrix coating
A. C.M.C.
B. Shellac
C. Stearyl alcohol
D. Bees wax
A. C.M.C.
B. Shellac
C. Stearyl alcohol
D. Bees wax
14. The diameter of the mesh aperture in the IP disintegration test apparatus is given below. Choose the correct size.
A. 2.00 mm
B. 4.00 mm
C. 1.00 mm
D. 1.50 mm
A. 2.00 mm
B. 4.00 mm
C. 1.00 mm
D. 1.50 mm
15. Schedule FF contains the list of the following
A. Drugs which can be marked under generic names only
B. Drugs which are habit forming
C. Standards for ophthalmic preparation
D. Drugs which are exempt from certain provisions applicable to manufacturing
A. Drugs which can be marked under generic names only
B. Drugs which are habit forming
C. Standards for ophthalmic preparation
D. Drugs which are exempt from certain provisions applicable to manufacturing
16. Gelatin I.P. should comply with
A. Limit test for chloride
B. Microbial limits
C. Limit test for sulphate
D. Sterlity test
17 Expiry period of drug preparations included in Schedule “P” of the Drugs & Cosmetics Rules 1945, cannot exceed –
A. 12 months from date of manufacture
B. 24 months from date of manufacture
C. 120 months from date of manufacture
D. 60 months from date of manufacture
A. 12 months from date of manufacture
B. 24 months from date of manufacture
C. 120 months from date of manufacture
D. 60 months from date of manufacture
18. Content uniformity test is used to ensure which of the following quantities?
A. Bioequivalency
B. Dissolution
C. Purity
D. Potency
A. Bioequivalency
B. Dissolution
C. Purity
D. Potency
19. Which of the following capsule size has the smallest capacity?
A. 5
B. 1
C. 0
D. 000
A. 5
B. 1
C. 0
D. 000
20. Oral liquids must comply with the following requirements –
A. Sterility test
B. Test for freedom from pathogenic organisms
C. Dissolution test
D. Pyrogen test
A. Sterility test
B. Test for freedom from pathogenic organisms
C. Dissolution test
D. Pyrogen test
21. Two drug products are considered bioequivalent if –
A. The rate and extent of systemic absorption is almost similar
B. They have been formulated in a similar manner
C. They are metabolized by the same route
D. They contain same amount of drug
A. The rate and extent of systemic absorption is almost similar
B. They have been formulated in a similar manner
C. They are metabolized by the same route
D. They contain same amount of drug
22. Standards of Patent and Proprietary medicines are contained in –
A. Schedule O of D & C Rules
B. Schedule P of D & C Rules
C. Schedule U of D & C Rules
D. Schedule V of D & C Rules
A. Schedule O of D & C Rules
B. Schedule P of D & C Rules
C. Schedule U of D & C Rules
D. Schedule V of D & C Rules
23. Schedule M of the Drugs and Cosmetics Rules contain –
A. Requirement of Good manufacturing practice
B. List of minimum equipments for efficient running of Pharmacy
C. Standards for surgical dressings
D. Particulars to be shown in manufacturing records
A. Requirement of Good manufacturing practice
B. List of minimum equipments for efficient running of Pharmacy
C. Standards for surgical dressings
D. Particulars to be shown in manufacturing records
24. Which of the following drugs can be marketed under generic name
A. Aspirin
B. Paracetamol
C. Ibuprofen
D. Diazepam
A. Aspirin
B. Paracetamol
C. Ibuprofen
D. Diazepam
25. In the mixing of thymol and menthol the following type of incompatibility occurs
A. Tolerance incompatibility
B. Therapeutic incompatibility
C. Physical incompatibility
D. Chemical incompatibility
A. Tolerance incompatibility
B. Therapeutic incompatibility
C. Physical incompatibility
D. Chemical incompatibility
SEE ANSWERS
ANSWERS OF PREVIOUS QUIZ 6
1. Ayurvedic, Siddha and Unani poisons2. Fosfestrol
3. Methotrexate
4. Diphenhydramine
5. Family pharmacist
6. Stage of delirium
7. Carpus luteum
8. 15 ml
9. Flumazenil
10. 30 min.
11. Magaldrate
12. Protamine sulfate
13. Phenylalanine
14. Standards for ophthalmic preparation
15. Standards for cosmetics
16. Holoenzyme
17. Pentoprazole
18. Transamination
19. Amiodarone
20. Cosmetics
21. Sodium-Potassium pump
22. Australia
23. Nicotinic acid
24. Chlorophores
25. President of PCI
