(a) Schedule O (b) Schedule R
(c) Schedule S (d) Schedule E
2. One of the following forms is needed for the cosmetic manufacture.
(a) Form 36 (b) Form 32
(c) Form 20 (d) Form 24
3. How many members are elected among themselves by registered pharmacist of state?
(a) Three (b) Four
(c) Five (d) Six
4. Nominated or elected members in “State Pharmacy Council” hold office for a term of
(a) Three years (b) Four years
(c) Five years (d) Six years
5. Pharmacy Act is established in
(a) 1948 (b) 1940
(c) 1995 (d) 1919
6. Which pharmaceutical product is not included in Schedule C?
(a) Toxins (b) Sera
(c) Antigen (d) Capsule
7. Names of drugs which shall be marketed under generic names only come under
(a) Schedule W (b) Schedule X
(c) Schedule Y (d) Schedule U
8. Pharmacy Council of India is doing all of below functions except
(a) To regulate minimum educational standard in pharmacy institute
(b) To prescribe the minimum standard of education required for registered as a pharmacist
(c) To compile and maintain central register for pharmacist
(d) To prescribe drug
9. Blood Bank comes under the schedule
(a) Schedule B (b) Schedule D
(c) Schedule F (d) Schedule G
10. Crocin is sale under
(a) Schedule H (b) Schedule G
(c) Schedule W (d) Schedule Y
11. “Ampicillin capsule should be used within 24 months.” This statement comes under
(a) Schedule C (b) Schedule R
(c) Schedule M (d) Schedule P
12. If the drug contains in filthy, putrid or decomposed substance then is known as
(a) Misbranded drug
(b) Adulterated drug
(c) Spurious drug
(d) Drug
13. Schedule M2 states that
(a) Requirements of factory premises for the manufacture of medical devices
(b) Requirements of factory premises for the manufacture of homeopathy
(c) Requirements of factory premises for the manufacture of cosmetics
(d) Requirements of factory premises for the manufacture of allopathy
14. Pharmacy Council of India has___________ state government nominated member(s)
(a) 1 (b) 2
(c) 3 (d) 4
15. In AICTE the chairman is appointed by
(a) State Government of Delhi
(b) Central Government
(c) Election of Registered Pharmacists
(d) President
16. In the “Joint State Pharmacy Council” elected member(s) among the Registered Pharmacists is/are
(a) 1 (b) 3
(c) 2 (d) 5
17. Manufacturing and analytical records of cosmetics are included in which schedule?
(a) Y (b) U
(c) U1 (d) V
18. Insulin injection according to Schedule P is should be stored
(a) At temperature 2˚C to 8 ˚C and it must not allow to freeze
(b) At temperature which not exceed 5°C
(c) At temperature which not exceed 20°C
(d) In cold place
19. Appendix II is about
(a) Number of animals for long-term toxicity studies
(b) Patient consent for participation in a Phase I clinical trial
(c) Format for submission of clinical trial reports
(d) Four groups of fixed dose combination and their data requirements
20. “Schedule F3” is related with
(a) Standard for surgical dressing
(b) Standard for sterilized umbilical tapes
(c) Standard for ophthalmic preparation
(d) Standard for production of sera
21. Spurious drug comes under
(a) Section 17 (b) Section 17A
(c) Section 17B (d) Section 3B
22. Insulin comes under
(a) Schedule H (b) Schedule J
(c) Schedule G (d) Schedule O
23. Form 20 states that
(a) Licenses to sell stock or exhibit or offer for sell or distribute by retail other than specified C, C1 and X.
(b) Licenses to sell stock or exhibit or offer for sell or distribute by wholesale other than specified C, C1
and X.
(c) Licenses to sell stock or exhibit or offer for sell or distribute by retail other than specified C, C1.
(d) Licenses to sell stock or offer for sell or redistribute by retail other than specified C, C1 and X
24. Application for grant of a licence to manufacture Ayurvedic, Sidhha or Unani drugs requires
(a) Form 24D (b) Form 25E
(c) Form 20 (d) Form 21
25. Private testing laboratory for carrying out tests on drugs requires
(a) Form 32 (b) Form 31
(c) Form 30 (d) Form 36
26. List of coal tar colours permitted to be used in cosmetics is covered under
(a) Schedule O (b) Schedule P
(c) Schedule Q (d) Schedule R
27. Schedule J is related to
(a) GMP
(b) Curable disease
(c) List of diseases and ailments which drug cannot claim.
(d) Pack sizes of drug.
28. Injection syringe and needle are covered under
(a) Schedule A (b) Schedule B
(c) Schedule C (d) Schedule D
29. “Dettol” comes under
(a) Schedule N (b) Schedule O
(c) Schedule P (d) Schedule Q
30. If blood group is “AB” then colour label used is
(a) Red (b) White
(c) Yellow (d) Blue
31. Schedule N states
(a) List of minimum equipment for efficient running of pharmacy
(b) List of minimum equipment required for manufacturing of drug
(c) Requirement of factory premises and hygienic condition to be complied
(d) Standard for cosmetics
32. Schedule C is related to
(a) List of Biological and Immunological product
(b) List of Homeopathy product
(c) List of Ayurvedic product
(d) List of Allopathic product
33. “Kala jadu or Kavach” comes under
(a) Schedule J (b) Schedule K
(c) Schedule L (d) Schedule P
34. Pharmacy Council of India contain comprises ______ member(s) from AICTE and UGC.
(a) 1
(b) 2
(c) 3
(d) 4
35. Proforma for sending memorandum is included in
which schedule?
(a) D (b) A
(c) FF (d) Q
36. The schedule in Drug and Cosmetics Act that deals with requirement and guidelines of clinical trial, import and manufacture of new drug is
(a) Schedule O (b) Schedule M
(c) Schedule F (d) Schedule Y
37. State Pharmacy Council should have the following number of elected members:
(a) Six (b) Five
(c) Nine (d) Seven
38. Schedule D as per D & C Act is concerned with
(a) List of drug exempted from the provision of import of drugs
(b) Disease or ailments which a drug may not purport to prevent or cure
(c) Requirement of factory premises
(d) List of prescription drugs
39. One of the following is/all are ex officio member(s) of State Pharmacy Council
(a) Chief pharmacist of government hospital
(b) Chief administrative medical officer of the state
(c) Assistant drug controller
(d) All
40. The Education Regulation is published in official gazette by
(a) Ministry of Education
(b) Central Government
(c) Drug Controller
(d) President, Pharmacy Council of India
41. List of drugs whole import, manufacture and sale, labelling and packaging are governed by special provisions are included in schedule
(a) X (b) K
(c) H (d) G
42. Biological and Biotechnological products are included in Schedule
(a) A (b) B
(c) C and C1 (d) X
43. Drug and Magic Remedies Act is enacted in
(a) 1954 (b) 1948
(c) 1985 (d) 1919
44. Diabetes comes under
(a) Schedule G (b) Schedule H
(c) Schedule D (d) Schedule J
45. Grant of licence to manufacture a drug requires
(a) Form 24 (b) Form 25
(c) Form 26 (d) Form 27
46. List of drugs which should be used by patient under medical supervision is covered under _______ as per D & C Act
(a) Schedule G (b) Schedule H
(c) Schedule I (d) Schedule J
47. As per D and C Act Schedule T states about
(a) Requirements of factory premises for the manufacture of medical devices
(b) Requirements of factory premises for the manufacture of Homeopathy drugs
(c) Requirements of factory premises for the manufacture of Ayurveda, Sidhha and Unani drugs
(d) Requirements of factory premises for the manufacture of Allopathy drugs
48. TGA is regulatory agency of _____________.
(a) Denmark (b) Austria
(c) Australia (d) Zimbabwe
49. MHRA is regulatory agency of ___________
(a) UK (b) Denmark
(c) Brazil (d) South Africa
50. Schedule _________ of Drugs and Cosmetics Act includes requirements and guidelines on clinical trials for import and manufacture of new drugs.
(a) W (b) X
(c) Y (d) V
51. For parenteral preparation in glass containers minimum area required is
(a) 250 square metres
(b) 400 square metres
(c) 500 square metres
(d) 150 square metres
52. MCC is regulatory agency of _____________
(a) UK
(b) Denmark
(c) Brazil
(d) South Africa
53. In State Pharmacy Council all following are ex officio members except
(a) President of India
(b) Chief Administrator Medical Officer of State
(c) The Officer In Charge of Drug Control Organization
(d) Government Analyst
54. Schedule X of Drugs and Cosmetics Act comprises
(a) List of incurable diseases
(b) Guidelines for clinical trials
(c) List of generic drugs
(d) None of the above
55. As per D and C Act “Schedule N” is related with
(a) List of maximum equipments for efficiently running pharmacy
(b) Area for opening retail pharmacy
(c) List of minimum equipment for efficiently running pharmacy
(d) Area required to open wholesale drug store
56. As per D & C Act “Schedule FF” is related with
(a) Parenteral preparation
(b) Ointment formulation
(c) Skin cosmetic preparation
(d) Ophthalmic preparation
57. Which of the following is prohibited to be imported?
(a) Toilet preparations
(b) Ayurvedic drugs
(c) Schedule ‘C’ and ‘G’ drugs
(d) Misbranded drugs
58. Hatch Waxman Act is related to
(a) Banned dugs
(b) Over-the-counter drugs
(c) Dangerous drugs
(d) Generic drugs
59. Coca, opium and hemp come under:
(a) Insecticide Act
(b) Poisons Act
(c) Dangerous Drugs Act
(d) Spurious Drug Act
60. The first edition of Indian Pharmacopoeia was published in the year:
(a) 1940
(b) 1950
(c) 1955
(d) 1985
61. Pharmacy Council of India is reconstituted:
(a) Every 2 Years
(b) Every 3 Years
(c) Every 5 Years
(d) Every 6 Years
62. In Phase-II trial following number of patient should be studied
(a) 10–12 patients
(b) 1–10 patients
(c) 100 patients
(d) 500 patients
63. Purpose of Phase-III trial is
(a) To determine maximum tolerated dose in humans, Pharmacodynamic effects, Adverse effects
(b) Determine Possible therapeutic uses, Effective doses range
(c) Efficacy and Ssafety of drug in larger number of patients (500 patients)
(d) Long time adverse effects after marketing drug
64. Standard for mechanical contraceptive comes under Schedule __________ as per D and C Act
(a) R
(b) R1
(c) S
(d) O
65. If drug is so coloured, coated or polished that damage its therapeutic value or it is made to appear of better or greater therapeutic value than it really is known as
(a) Adulterated Drug
(b) Spurious Drug
(c) Misbranded Drug
(d) True Drug
66. Patent Act is established in
(a) 1948 (b) 1940
(c) 1970 (d) 1919
67. Pack size of drug is covered under
(a) Schedule P (b) Schedule R
(c) Schedule P1 (d) Schedule O
68. For licence granted to sell by retail drugs, specified in schedule C and C(I) drugs form no. require is
(a) 20 (b) 20B
(c) 21 (d) 21B
69. As per Schedule P Carbenicillin Sodium Powder should be stored in/at
(a) A cool place
(b) A cold place
(c) Temperature not exceeding 5°C
(d) Well closed container, Protect from light, in cool place, protect from light
70. DTAB has __________ ex officio members.
(a) Five (b) Six
(c) Four (d) Eight
71. For Schedule X drug use of Human beings Special Labelling requirement require is
(a) Symbol X given in red
(b) Symbol N in red displayed on left top corner of the label
(c) Symbol N displayed on left top corner of the label
(d) Symbol H displayed on right top corner of the label
72. Aspirin sodium comes under
(a) Schedule G (b) Schedule H
(c) Schedule J (d) Schedule W
73. Example of Schedule G drug is
(a) Metformin (b) Enalapril
(c) Cefuroxime (d) Barbital
74. In 1954 one of the following act is passed
(a) Narcotic and Psychotropic Substance Act
(b) Drug and Magic Remedies Act
(c) The Medical Termination of Pregnancy Act
(d) Poisonous Act
75. Post marketing Surveillance comes under clinical trail
(a) Phase I (b) Phase II
(c) Phase III (d) Phase V
Answer Keys
1. (a) 2. (b) 3. (d) 4. (c) 5. (a) 6. (d) 7. (a) 8. (d) 9. (c) 10. (c) 11. (d) 12. (b) 13. (c) 14. (a) 15. (b) 16. (b) 17. (c) 18. (a) 19. (c) 20. (b) 21. (c) 22. (c) 23. (a) 24. (a) 25. (d) 26. (c) 27. (c) 28. (c) 29. (b) 30. (b) 31. (a) 32. (a) 33. (a) 34. (a) 35. (b) 36. (d) 37. (a) 38. (a) 39. (d) 40. (b) 41. (a) 42. (c) 43. (a) 44. (d) 45. (b) 46. (a) 47. (c) 48. (c) 49. (a) 50. (c) 51. (a) 52. (d) 53. (a) 54. (d) 55. (c) 56. (d) 57. (d) 58. (d) 59. (c) 60. (c) 61. (c) 62. (a) 63. (c) 64. (b) 65. (c) 66. (c) 67. (c) 68. (c) 69. (c) 70. (d) 71. (b) 72. (d) 73. (a) 74. (b) 75. (d)