Explore topic-wise MCQs in GPAT.

This section includes 925 Mcqs, each offering curated multiple-choice questions to sharpen your GPAT knowledge and support exam preparation. Choose a topic below to get started.

301.

The Rheogram of thixotropic material determined by...................

A. Duration through which sample is exposed to any one shear rate.
B. Rate at which shear increased or decreased.
C. Both of the above
D. None of the above
Answer» D. None of the above
302.

Stability testing is done

A. to determine shelf life of product
B. to determine the components used for packaging
C. to get information at preformulation stage
D. All of the above
Answer» E.
303.

Which of the following is a psychotropic substance under the Narcotic Drugs andPsychotropic Susbtances Act?

A. Barbital (barbiturate)
B. Ampicillin (antibiotic)
C. Albendazole (anti parasitic)
D. Chloroquine (anti malarial)
Answer» B. Ampicillin (antibiotic)
304.

Which of the following is a ‘Patent or Proprietary Ayurvedic/Siddha/Unani Medicine’ according to Drugs and Cosmetics Act?

A. Parachute coconut oil
B. Amrutanjan Balm
C. Odomos insect repellent cream
D. Arnica hair oil
Answer» C. Odomos insect repellent cream
305.

A company wishes to advertise for a new emergency oral contraceptive that it has introduced in the market-

A. Advertisement of oral contraceptives is not allowed as per DMR (OA) act
B. The company can seek permission from the Government to advertise
C. Advertisements for oral contraceptives is allowed as per DMR (OA) act
D. The advertisement has to be sent confidentially only to a Registered Medical Practitioner.
Answer» C. Advertisements for oral contraceptives is allowed as per DMR (OA) act
306.

Prepared opium

A. is an extract suitable for smoking
B. is any medicine containing opium
C. is also called as hemp
D. has undergone the processes to adapt it for medicinal use
Answer» B. is any medicine containing opium
307.

The Pharmacy Council of India “Education Regulations’ for the Diploma Course inPharmacy, that is currently in force, was passed in the year

A. 1981
B. 1985
C. 1991
D. 1995
Answer» D. 1995
308.

The First Schedule to the Drugs and Cosmetics Act, 1940 prescribes

A. standards for cosmetics
B. standards for medical devices
C. authoritative books of Ayurvedic, Sidhha and Unani Tibb system
D. standards of the drugs to be complied with by imported drugs
Answer» D. standards of the drugs to be complied with by imported drugs
309.

Minimum area of the shop to obtain a wholesale licence to sell and stock drugs shallbe

A. five square metres
B. ten square metres
C. fifteen square metres
D. twenty square metres
Answer» D. twenty square metres
310.

The schedules to the Drugs and Cosmetics Act are

A. A to Y
B. First and Second
C. 1 to 25
D. A and B only
Answer» C. 1 to 25
311.

Who among the following is the Chairman of Drug Technical Advisory Board?

A. The Drugs Controller of India
B. The President of Pharmacy Council of India
C. The President of Medical Council of India
D. The Director General of Health Services
Answer» E.
312.

What is the definition of a “Magic Remedy*?

A. talisman, mantra, kavacha or any other charm or any substance alleged to possess miraculous powers powers to diagnose, cure, mitigate, treat or prevent a disease in humans or animals
B. Any substance natural or synthetic or any salt or preparation of such substance or material, included in the list of psychotropic substances specified in the
C. Any substance, whether processed, partially processed or unprocessed, which is intended for human consumption.
D. Ethyl alcohol of any strength and purity having the chemical composition C2H5OH
Answer» B. Any substance natural or synthetic or any salt or preparation of such substance or material, included in the list of psychotropic substances specified in the
313.

Which of the following is a ‘drug’ as per the law?

A. Empty gelatin capsules, bandages and insect repellent creams
B. Energy drinks and candy bars
C. Mouth freshening spearmint chewing gum
D. Fish and Chicken
Answer» B. Energy drinks and candy bars
314.

Who has the power to fix the ceiling price of scheduled formulations?

A. State Government
B. Central Government
C. Lok Sabha
D. Rajya Sabha
Answer» C. Lok Sabha
315.

Which of the following drug product will have N℞ on its label

A. Antihypertensive drug (ẞ- blocker)
B. Antimicrobial drug (Chloroquine)
C. Narcotic analgesic (Morphine)
D. Antidiabetic (Glibenclamide)
Answer» D. Antidiabetic (Glibenclamide)
316.

Schedule K pertains to

A. List of drugs that can be used with caution under medical supervision
B. List of drugs exempted from certain provisions governing import of drugs
C. List of drugs exempted from certain provisions governing manufacture and sale of drugs
D. List of diseases that a drug cannot claim to cure
Answer» D. List of diseases that a drug cannot claim to cure
317.

Under the Medicinal and Toilet Preparations (Excise Duties) Act, manufacture of anydutiable goods without a valid licence is punishable with

A. imprisonment up to six years or fine of twenty thousand rupees or both
B. imprisonment up to six months or fine of two thousand rupees or both
C. imprisonment up to six months or fine of twenty thousand rupees or both
D. imprisonment up to six years or fine of two thousand rupees or both
Answer» C. imprisonment up to six months or fine of twenty thousand rupees or both
318.

According to provisions given under NDPS Act, 1985

A. Opium and Coca cultivation and gathering can be permitted and regulated only by Central Government
B. Opium and Coca cultivation and gathering can be regulated and permitted both by Central and State Governments
C. Cannabis consumption can be regulated only by Central Government
D. Manufacture of medicinal opium is to be done only by state Government.
Answer» B. Opium and Coca cultivation and gathering can be regulated and permitted both by Central and State Governments
319.

The main object of the Pharmacy Act, 1948 is to

A. control the advertisement of drugs
B. regulate the profession of pharmacy
C. prevent the infliction of unnecessary pain or suffering on animals
D. regulate the sale of narcotic drugs and psychotropic substances
Answer» C. prevent the infliction of unnecessary pain or suffering on animals
320.

A nonbonded manufactory shall be inspected by the officer at least

A. once every month
B. once every two months
C. once every six months
D. once every year
Answer» B. once every two months
321.

Officer under FSSAI-

A. Government Analyst
B. Public Analyst
C. Drug Controller
D. none
Answer» B. Public Analyst
322.

Compulsory Licence is issued when

A. A drug is novel
B. Forms the first line of treatment for a disorder or disease
C. Is exorbitantly priced
D. Supply is insufficient
Answer» D. Supply is insufficient
323.

Plant of the species of Papaver, from which opium or any phenanthrene alkaloid canbe extracted, is called

A. opium poppy
B. coca
C. heroin
D. Cannabis sativam
Answer» B. coca
324.

Which of the following is/are non-patentable

A. A new medical device for diagnosis
B. Admixture of two known substances to give a new effect
C. Algorithms
D. A genetically modified microorganism
Answer» D. A genetically modified microorganism
325.

According to definition of ‘Food’, following are classified as food

A. Mouthwash and toothpaste
B. Protein supplements and Packaged drinking water
C. Hajmola Candy and Halls candy
D. Live animals (fish, chicken and goat)
Answer» C. Hajmola Candy and Halls candy
326.

Which of the following words/particulars are necessary to be included in the labellingof Schedule G drugs for oral use

A. NOT FOR INJECTION
B. Warning: If irritation persists or increases, discontinue use and consult physician.
C. For External Use Only
D. A vertical redline on the left side of the label
Answer» E.
327.

The Narcotic Drugs and Psychotropic Substances Act was passed in the year

A. 1940
B. 1955
C. 1985
D. 2000
Answer» D. 2000
328.

Which of the following is not an objective of bioavailability studies?

A. Primary stages of development of suitable dosage form for new drug
B. Determination of the influence of excipients, patient-related factors, etc
C. Development of new formulations of the existing drugs
D. Control the quantity of the drug to be administered
Answer» E.
329.

Salts improve solubility and dissolution characteristics.

A. True
B. False
C. none
D. all
Answer» B. False
330.

…………..it represents the degree to which a drug is distributed in body tissue rather than

A. Volume of distribution (YD)
B. Effect of distribution
C. Area of distribution
D. None of the above
Answer» B. Effect of distribution
331.

According to the pH-partition hypothesis which one of the given options doesn’t govern theabsorption?

A. The molecular size of the drug
B. PH at the absorption site
C. Lipid solubility of unionized drugs
D. Dissociation constant
Answer» B. PH at the absorption site
332.

Binding of drugs falls into 2 components those are _______________

A. Binding of drugs to blood components and to extravascular tissue
B. Binding of drugs to blood components and to other cells
C. Binding of drugs to cells and blood cells
D. Binding of drugs to blood components to bones and cells
Answer» B. Binding of drugs to blood components and to other cells
333.

Which of the following is not a form of excipients?

A. Paracetamol
B. Disintegrants
C. Lubricants
D. Binders
Answer» B. Disintegrants
334.

Each face of the crystal has a different interfacial barrier.

A. True
B. False
C. none
D. all
Answer» B. False
335.

The ratio of maximum safe concentration to minimum effective concentration is called as

A. Therapeutic index
B. Therapeutic range
C. Therapeutic outcome
D. Therapeutic ratio
Answer» B. Therapeutic range
336.

Diffusion coefficient of drug D, Greater the value faster us the dissolution.

A. True
B. False
C. none
D. all
Answer» B. False
337.

The rate of drug bioavailability is most rapid when the drug is formulated as a…..

A. controlled released product
B. hard gelatin capsule
C. tablet
D. solution
Answer» E.
338.

What is the molecular weight of human serum albumin?

A. 5000 Dalton
B. 65,000 Dalton
C. 60,000 Dalton
D. 75,000 Dalton
Answer» C. 60,000 Dalton
339.

How can we study the gastric emptying of a given drug?

A. By mixing the colour with the drug
B. Waiting for the subject man to throw-up
C. Tagging the drug with a radioisotope and scanning the stomach
D. Waiting for the patient to pass feces
Answer» D. Waiting for the patient to pass feces
340.

What is meant by elimination half-life?

A. Time take for half of the amount of drug to get completely eliminated from only the organs
B. Time take for half of the amount of drug to get completely eliminated from only blood
C. Time take for half of the amount of drug to get completely eliminated from only plasma
D. Time take for half of the amount of drug to get completely eliminated from the body as well as plasma
Answer» E.
341.

………..change in drug kinetics is known as chronokinetics.

A. Time-dependent
B. Dose-dependent
C. Both (a) & (b)
D. None of the above
Answer» B. Dose-dependent
342.

When the solvent molecules are entrapped in the crystalline structure of the polymorph, it is called as

A. Pseudo-polymorphism
B. Amorphism
C. Crystallinity
D. All of the above
Answer» B. Amorphism
343.

Which of the following is initial step for drug absorption in case of tablet dosage form?

A. Friability
B. Disintegration
C. Dissolution
D. None of these
Answer» C. Dissolution
344.

If the Relative Bioavailability is 1, it indicates:

A. Bioavailability of dosage form of one drug is same as that of the other dosage form
B. Complete binding of the drugs to the proteins as compared to the standard drug
C. Complete bioavailability of the drug
D. Complete distribution of the drug
Answer» B. Complete binding of the drugs to the proteins as compared to the standard drug
345.

Patient-related factors of drug absorption do not deal with which one of these?

A. Age
B. Gastric Emptying time
C. Intestinal transit time
D. Pharmaceutic ingredients
Answer» E.
346.

Which one of the following factors related to protein-drug binding is not related to drugs?

A. Physicochemical characteristics of a drug
B. The concentration of the drug in the body
C. The affinity of the drug for binding
D. Number of binding sites on the binding agent
Answer» E.
347.

Who has poorly developed BBB?

A. Infants
B. Adults Of age more than 20
C. Aged
D. Children at puberty
Answer» B. Adults Of age more than 20
348.

Which drugs accumulate in liver?

A. Acidic drugs like imipramine
B. Basic drugs like imipramine
C. Halogenated hydrocarbons
D. Chloroquinine
Answer» C. Halogenated hydrocarbons
349.

The total solid surface area of any particle is known as ___________

A. Absolute surface area
B. Effective surface area
C. Total surface area
D. Surface area
Answer» B. Effective surface area
350.

Which of the following is used in solid solutions method of enhancing bioavailability?

A. Highly water-soluble compound
B. Organic solvent
C. Inorganic clays like bentonite
D. Creating metastable polymorphs
Answer» B. Organic solvent