Blog

Pharmaceutical Jurisprudence MCQ: 30 Best Free Questions with Answers

Pharmaceutical jurisprudence MCQ practice is a quick way to pick up marks, because the questions are about years, schedules, forms and authorities. This quiz has 30 questions on the Drugs and Cosmetics Act, Pharmacy Act, NDPS Act and related laws.

Jurisprudence is also a very important subject for Drug Inspector and state pharmacist exams, so the facts you learn here will be useful beyond your college exam.

Take the Pharmaceutical Jurisprudence MCQ test now

This set has 30 questions and takes about 15 minutes. Do it once honestly, then read the explained questions below.

Pharmacy Quiz 5 - Pharmaceutical Jurisprudence

1 / 30

The Drugs and Cosmetics Act was enacted in the year

2 / 30

The Pharmacy Act was enacted in the year

3 / 30

The Pharmacy Act 1948 mainly regulates

4 / 30

The Pharmacy Council of India is constituted under the

5 / 30

The NDPS Act was passed in the year

6 / 30

The Drugs and Magic Remedies (Objectionable Advertisements) Act was passed in

7 / 30

The Drugs (Prices Control) Order is issued under the

8 / 30

NPPA stands for

9 / 30

Schedule H drugs can be sold only

10 / 30

Schedule X of the Drugs and Cosmetics Rules deals with

11 / 30

Schedule G drugs carry a label warning stating

12 / 30

Schedule M of the Drugs and Cosmetics Rules deals with

13 / 30

Schedule P deals with

14 / 30

Schedule Y deals with

15 / 30

The Drugs Technical Advisory Board advises

16 / 30

CDSCO is headed by the

17 / 30

The minimum qualification for registration as a pharmacist in India is

18 / 30

A licence in Form 20B is issued for

19 / 30

A manufacturing licence for drugs other than Schedule C, C1 and X is issued in

20 / 30

Cannabis and opium are regulated in India by the

21 / 30

Records of sale of Schedule H drugs must be kept for

22 / 30

The Pharmacy Practice Regulations 2015 were framed by the

23 / 30

A patent granted in India is valid for

24 / 30

The Indian Patents Act was enacted in the year

25 / 30

The Medical Termination of Pregnancy Act was passed in

26 / 30

CPCSEA is concerned with

27 / 30

The Consumer Protection Act of 2019 replaced the Act of

28 / 30

A spurious drug is one that

29 / 30

Schedule C of the Drugs and Cosmetics Rules includes

30 / 30

Schedule F of the Drugs and Cosmetics Rules relates to

Your score is

The average score is 0%

What makes Pharmaceutical Jurisprudence tricky for students

Jurisprudence is a number and keyword subject. You must remember which law was passed in which year, what each schedule deals with and which form is used for which licence. The good news is that the list is limited. If you make one table of Act, year and purpose and one table of schedules, you can cover most MCQs in a few days.

Five Pharmaceutical Jurisprudence MCQ questions that confuse students

These are the questions from the set above that students most often get wrong, with the reason behind each answer.

  1. Which schedule deals with Good Manufacturing Practices?
    Answer: Schedule M. Schedule Y is for clinical trials and Schedule P is for the life period of drugs. Students often mix these letters.
  2. For how long must records of Schedule H drug sales be kept?
    Answer: 3 years. Keep this with the fact that Schedule H drugs are sold only on the prescription of a registered medical practitioner.
  3. Which Act regulates cannabis and opium in India?
    Answer: The NDPS Act, 1985. It is not the Drugs and Cosmetics Act. NDPS stands for Narcotic Drugs and Psychotropic Substances.
  4. What is a licence in Form 20B used for?
    Answer: Wholesale of drugs other than Schedule C and C1 drugs. A manufacturing licence for drugs other than Schedule C, C1 and X is in Form 25.
  5. What is a spurious drug?
    Answer: A drug that imitates or is substituted for another drug. Misbranded and adulterated drugs are different terms, so read the definitions carefully.

Small facts that win marks in Pharmaceutical Jurisprudence

  • The Drugs and Cosmetics Act was enacted in 1940, the Pharmacy Act in 1948, the Drugs and Magic Remedies Act in 1954 and the NDPS Act in 1985.
  • The Pharmacy Council of India is constituted under the Pharmacy Act, 1948.
  • The DPCO is issued under the Essential Commodities Act, 1955, and NPPA works on drug prices.
  • Schedule C covers biological products such as sera and vaccines, and Schedule X covers psychotropic drugs needing special prescription records.
  • CDSCO is headed by the Drugs Controller General of India (DCGI).
  • A patent in India is valid for 20 years, and the Patents Act was enacted in 1970.

How to get the most out of this practice set

Prepare two simple tables. The first has Act, year and main purpose. The second has schedule letter and its subject. Revise them every morning for one week and attempt this pharmaceutical jurisprudence MCQ quiz again at the end. Your score usually jumps because jurisprudence rewards repetition more than understanding.

Frequently asked questions about pharmaceutical jurisprudence MCQ

Is jurisprudence important for Drug Inspector exams?

Yes. Drugs and Cosmetics Act and Rules, NDPS Act and the Pharmacy Act form a large part of the Drug Inspector syllabus.

How many schedules should I remember?

Focus on A, C, C1, F, G, H, H1, M, P, X and Y first. These are asked most often.

Are laws updated often?

Rules and schedules are amended from time to time. Always check the latest notifications on the official CDSCO website before your exam.

Keep practising

If this pharmaceutical jurisprudence MCQ set felt comfortable, move on to the next subject. These pages will help:

For official syllabus details and regulations, refer to CDSCO and Pharmacy Council of India.

Written by the Noteskarts pharmacy education team. This quiz is for exam practice and learning only; always check your latest syllabus and standard textbooks for final answers.

Noteskarts

Hello Welcome to Noteskarts. I hop this article help you. thank you for visit.

Leave a Reply