CLASS DEKHNE K LIYE CLICK KAREIN

1. Which schedule contains different types of

forms in Drugs and Cosmetics Act, 1945
(a) Schedule B
(b) Schedule C
(c) Schedule D
(d) Schedule A
1. Which schedule contains different types of
forms in Drugs and Cosmetics Act, 1945
(a) Schedule B
(b) Schedule C
(c) Schedule D
(d) Schedule A
SCHEDULES TO THE RULES
• A- Performa for application for the licenses, issues and renewal of licenses, for
sending memoranda under the act.
• B-Rates of fee for test or analysis by the Central Drugs Laboratory or the state
drug laboratories.
• B1 - Fee for the test or analysis by the pharmacopeia laboratory for Indian
medicine or the govt. analyst.
2. Which Schedule gives information about fees for
test or analysis by the central drugs laboratories or
state drugs laboratories
(a) Schedule F
(b) Schedule Y
(c) Schedule K
(d) Schedule B
2. Which Schedule gives information about fees for
test or analysis by the central drugs laboratories or
state drugs laboratories
(a) Schedule F
(b) Schedule Y
(c) Schedule K
(d) Schedule B
SCHEDULES TO THE RULES
• A- Performa for application for the licenses, issues and renewal of licenses, for
sending memoranda under the act.
• B-Rates of fee for test or analysis by the Central Drugs Laboratory or the state
drug laboratories.
• B1 - Fee for the test or analysis by the pharmacopeia laboratory for Indian
medicine or the govt. analyst.
3. Biological and Biotechnological products are
included in IMP
(a) Schedule A
(b) Schedule B
(c) Schedule X
(d) Schedule C & C1
3. Biological and Biotechnological products are
included in
(a) Schedule A
(b) Schedule B
(c) Schedule X
(d) Schedule C & C1
SCHEDULES TO THE RULES
• C - List of biological and other special products whose import, sale,
distribution and manufacture are governed by special provision.
• C1 - List of other special products whose import, sale, distribution and
mfg are governed by special provision.
• D - List of drugs exempted from the provisions to import of drugs.
4. Schedule C and C1 of Drugs and Cosmetics
Act deals with
(a) List of biological and special products
(b) Management of wholesale pharmacy
(c) Dyes and pigments in cosmetics
(d) Management of retail pharmacy
4. Schedule C and C1 of Drugs and Cosmetics
Act deals with
(a) List of biological and special products
(b) Management of wholesale pharmacy
(c) Dyes and pigments in cosmetics
(d) Management of retail pharmacy
SCHEDULES TO THE RULES
• C - List of biological and other special products whose import, sale,
distribution and manufacture are governed by special provision.
• C1 - List of other special products whose import, sale, distribution and
mfg are governed by special provision.
• D - List of drugs exempted from the provisions to import of drugs.
5. Which one of the following comes under the
schedule C of the Drugs and Cosmetics
(a) OTC products
(b) Drugs from digitalis
(c) Biological products
(d) Surgical dressings
5. Which one of the following comes under the
schedule C of the Drugs and Cosmetics
(a) OTC products
(b) Drugs from digitalis
(c) Biological products
(d) Surgical dressings
SCHEDULES TO THE RULES
• C - List of biological and other special products whose import, sale,
distribution and manufacture are governed by special provision.
• C1 - List of other special products whose import, sale, distribution and
mfg are governed by special provision.
• D - List of drugs exempted from the provisions to import of drugs.
6. Schedule D in Drugs and Cosmetics Act refers
to
(a) List of poisonous substances
(b) Standards for surgical dressing
(c) List of drugs exempted from certain
manufacturing provisions
(d) List of drugs exempted from import provision
6. Schedule D in Drugs and Cosmetics Act refers
to
(a) List of poisonous substances
(b) Standards for surgical dressing
(c) List of drugs exempted from certain
manufacturing provisions
(d) List of drugs exempted from import provision
SCHEDULES TO THE RULES
• C - List of biological and other special products whose import, sale,
distribution and manufacture are governed by special provision.
• C1 - List of other special products whose import, sale, distribution and
mfg are governed by special provision.
• D - List of drugs exempted from the provisions to import of drugs.
7. Poisonous drugs are covered in
(a) Schedule E1
(b) Schedule Y
(c) Schedule F
(d) Schedule X
7. Poisonous drugs are covered in
(a) Schedule E1
(b) Schedule Y
(c) Schedule F
(d) Schedule X
SCHEDULES TO THE RULES
• E1 - List of poisonous substances under the Ayurvedic (including Siddha) and Unani
systems of medicine.
• F - Requirement for the functioning and operation of the blood bank and/or for
preparation of blood components.
• F1 -
• Part I - Provisions applicable to the production of all bacterial and viral vaccine.
• Part II - Provisions applicable to the production of all sera from living animal of
blood components.
• Part III - Provisions applicable to the manufacture and standardization of
diagnostic agents (Bacterial origin)
8. Schedule F means
(a) Regulations and standards for surgical
dressings
(b) Regulations and standards for umbilical
tapes
(c) Regulations and standards for vaccines
(d) Regulations and standards for running a
blood bank
8. Schedule F means
(a) Regulations and standards for surgical
dressings
(b) Regulations and standards for umbilical
tapes
(c) Regulations and standards for vaccines
(d) Regulations and standards for running a
blood bank
SCHEDULES TO THE RULES
• E1 - List of poisonous substances under the Ayurvedic (including Siddha) and Unani
systems of medicine.
• F - Requirement for the functioning and operation of the blood bank and/or for
preparation of blood components.
• F1 -
• Part I - Provisions applicable to the production of all bacterial and viral vaccine.
• Part II - Provisions applicable to the production of all sera from living animal of
blood components.
• Part III - Provisions applicable to the manufacture and standardization of
diagnostic agents (Bacterial origin)
9. Which schedule is standards for surgical
dressing
(a) Schedule D
(b) Schedule F1
(c) Schedule F2
(d) Schedule F3
9. Which schedule is standards for surgical
dressing
(a) Schedule D
(b) Schedule F1
(c) Schedule F2
(d) Schedule F3
• F2 - Standards for surgical dressings.
• F3 -Standards for sterilized umbilical tapes.
• FF- Standards of ophthalmic preparations.
10. Under the Drugs and Cosmetics Rules
1945, Schedule ____ gives standards for
umbilical tapes
(a) M II
(b) M III
(c) F II
(d) F III
10. Under the Drugs and Cosmetics Rules
1945, Schedule ____ gives standards for
umbilical tapes
(a) M II
(b) M III
(c) F II
(d) F III
• F2 - Standards for surgical dressings.
• F3 -Standards for sterilized umbilical tapes.
• FF- Standards of ophthalmic preparations.
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11. Under Drugs and Cosmetics Act, 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
11. Under Drugs and Cosmetics Act, 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
• F2 - Standards for surgical dressings.
• F3 -Standards for sterilized umbilical tapes.
• FF- Standards of ophthalmic preparations.
12. Schedule for medications under
supervision of RMP
(a) T
(b) H
(c) S
(d) G
12. Schedule for medications under
supervision of RMP
(a) T
(b) H
(c) S
(d) G
• G - List of substances that are required to be used only under medical
supervision and which are to be labeled accordingly.
• H - List of prescription drugs.
• J - Disease or ailments which a drug may not purport to prevent or cure.
• K - Drugs exempted from certain provision relating to manufacture of
drugs.
• L -1 Good laboratory practice (GLP) and requirement of premises and
equipment.
• M - Good manufacturing practice (GMP) requirement of factory
premises, plants and equipment.
13. The words "It is dangerous to take this
preparation except under medical supervision” can
be found on label of drugs belonging to
(a) Schedule X
(b) Schedule H
(c) Schedule C
(d) Schedule G
13. The words "It is dangerous to take this
preparation except under medical supervision” can
be found on label of drugs belonging to
(a) Schedule X
(b) Schedule H
(c) Schedule C
(d) Schedule G
• G - List of substances that are required to be used only under medical
supervision and which are to be labeled accordingly.
• H - List of prescription drugs.
• J - Disease or ailments which a drug may not purport to prevent or cure.
• K - Drugs exempted from certain provision relating to manufacture of
drugs.
• L -1 Good laboratory practice (GLP) and requirement of premises and
equipment.
• M - Good manufacturing practice (GMP) requirement of factory
premises, plants and equipment.
14. Prescription drugs are given under which
schedule of Drugs and Cosmetics Rules
(a) Schedule K
(b) Schedule H
(c) Schedule R
(d) Schedule M
14. Prescription drugs are given under which
schedule of Drugs and Cosmetics Rules
(a) Schedule K
(b) Schedule H
(c) Schedule R
(d) Schedule M
• G - List of substances that are required to be used only under medical
supervision and which are to be labeled accordingly.
• H - List of prescription drugs.
• J - Disease or ailments which a drug may not purport to prevent or cure.
• K - Drugs exempted from certain provision relating to manufacture of
drugs.
• L -1 Good laboratory practice (GLP) and requirement of premises and
equipment.
• M - Good manufacturing practice (GMP) requirement of factory
premises, plants and equipment.
15. Which of the following drug must to be sold
by retail only after producing a prescription by
a registered medical practitioner
(a) Schedule H
(b) Schedule G
(c) Schedule X
(d) Schedule M
15. Which of the following drug must to be sold
by retail only after producing a prescription by
a registered medical practitioner
(a) Schedule H
(b) Schedule G
(c) Schedule X
(d) Schedule M
• G - List of substances that are required to be used only under medical
supervision and which are to be labeled accordingly.
• H - List of prescription drugs.
• J - Disease or ailments which a drug may not purport to prevent or cure.
• K - Drugs exempted from certain provision relating to manufacture of
drugs.
• L -1 Good laboratory practice (GLP) and requirement of premises and
equipment.
• M - Good manufacturing practice (GMP) requirement of factory
premises, plants and equipment.
16. List of diseases and ailments which a drug
may not purport to prevent or cure or make
claims to prevent or cure under the Drugs and
Cosmetics Rule 1945 is given under
(a) Schedule J
(b) Schedule K
(c) Schedule M
(d) Schedule P
16. List of diseases and ailments which a drug
may not purport to prevent or cure or make
claims to prevent or cure under the Drugs and
Cosmetics Rule 1945 is given under
(a) Schedule J
(b) Schedule K
(c) Schedule M
(d) Schedule P
• G - List of substances that are required to be used only under medical
supervision and which are to be labeled accordingly.
• H - List of prescription drugs.
• J - Disease or ailments which a drug may not purport to prevent or cure.
• K - Drugs exempted from certain provision relating to manufacture of
drugs.
• L -1 Good laboratory practice (GLP) and requirement of premises and
equipment.
• M - Good manufacturing practice (GMP) requirement of factory
premises, plants and equipment.
17. Good laboratory practices and
requirements of premises and equipment is
specified in
(a) Schedule M
(b) Schedule N
(c) Schedule L-1
(d) Schedule M-1
17. Good laboratory practices and
requirements of premises and equipment is
specified in
(a) Schedule M
(b) Schedule N
(c) Schedule L-1
(d) Schedule M-1
• G - List of substances that are required to be used only under medical
supervision and which are to be labeled accordingly.
• H - List of prescription drugs.
• J - Disease or ailments which a drug may not purport to prevent or cure.
• K - Drugs exempted from certain provision relating to manufacture of
drugs.
• L-1 Good laboratory practice (GLP) and requirement of premises and
equipment.
• M - Good manufacturing practice (GMP) requirement of factory
premises, plants and equipment.
18. In the Drugs and Cosmetics Act and Rules,
the schedule relating to GMP is
(a) Schedule X
(b) Schedule P
(c) Schedule M
(d) Schedule Y
18. In the Drugs and Cosmetics Act and Rules,
the schedule relating to GMP is
(a) Schedule X
(b) Schedule P
(c) Schedule M
(d) Schedule Y
M - Good manufacturing practice (GMP) requirement of factory premises,
plants and equipment.
• M ₁ - Requirement of factory premises etc. for manufacture of
homoeopathic preparation
• M₂ - Requirement of factory premises etc. for manufacture of
cosmetics.
• M3 - Requirements of factory premises for the manufacture of
medical devices.
19. The schedule for good manufacturing
practices and requirements of factory premises
for the manufacture of belongs to
(a) Schedule X
(b) Schedule W
(c) Schedule L
(d) Schedule M
19. The schedule for good manufacturing
practices and requirements of factory premises
for the manufacture of belongs to
(a) Schedule X
(b) Schedule W
(c) Schedule L
(d) Schedule M
M - Good manufacturing practice (GMP) requirement of factory premises,
plants and equipment.
• M ₁ - Requirement of factory premises etc. for manufacture of
homoeopathic preparation
• M₂ - Requirement of factory premises etc. for manufacture of
cosmetics.
• M3 - Requirements of factory premises for the manufacture of
medical devices.
20. Schedule M1 of Drugs and Cosmetics Act
1940 & Rules 1945 deals with
(a) Allopathic medicines
(b) Homeopathic medicines
(c) Medical devices
(d) Cosmetics
20. Schedule M1 of Drugs and Cosmetics Act
1940 & Rules 1945 deals with
(a) Allopathic medicines
(b) Homeopathic medicines
(c) Medical devices
(d) Cosmetics
M - Good manufacturing practice (GMP) requirement of factory premises,
plants and equipment.
• M ₁ - Requirement of factory premises etc. for manufacture of
homoeopathic preparation
• M₂ - Requirement of factory premises etc. for manufacture of
cosmetics.
• M3 - Requirements of factory premises for the manufacture of
medical devices.
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21. The version of GMP in India that describe
requirement of factory premises for
manufacture of cosmetics
(a) Schedule-M
(b) Schedule-M III
(c) Schedule-M II
(d) Schedule -MI
21. The version of GMP in India that describe
requirement of factory premises for
manufacture of cosmetics
(a) Schedule-M
(b) Schedule-M III
(c) Schedule-M II
(d) Schedule -MI
M - Good manufacturing practice (GMP) requirement of factory premises,
plants and equipment.
• M ₁ - Requirement of factory premises etc. for manufacture of
homoeopathic preparation
• M₂ - Requirement of factory premises etc. for manufacture of
cosmetics.
• M3 - Requirements of factory premises for the manufacture of
medical devices.
22. List of minimum equipment for efficient
running of a pharmacy is given in Schedule
(a) M
(b) N
(c) Q
(d) R
22. List of minimum equipment for efficient
running of a pharmacy is given in Schedule
(a) M
(b) N
(c) Q
(d) R
• N - List of minimum equipment for efficient running of a
pharmacy.
• O - Standard for disinfectant fluid.
• P - Life period of drug.
• P₁ - Pack sizes of drugs.
23. Which of the following schedules to the
Drug and Cosmetics Rules refers to
requirements for a pharmacy
(a) Schedule M
(b) Schedule N
(c) Schedule O
(d) Schedule P
23. Which of the following schedules to the
Drug and Cosmetics Rules refers to
requirements for a pharmacy
(a) Schedule M
(b) Schedule N
(c) Schedule O
(d) Schedule P
• N - List of minimum equipment for efficient running of a
pharmacy.
• O - Standard for disinfectant fluid.
• P - Life period of drug.
• P₁ - Pack sizes of drugs.
24. A modern drug store should fulfil all
minimum requirements as specified in the
Drugs and Cosmetics Act 1940 and Rules 1945
(a) Schedule M
(b) Schedule N
(c) Schedule P
(d) Schedule S
24. A modern drug store should fulfil all
minimum requirements as specified in the
Drugs and Cosmetics Act 1940 and Rules 1945
(a) Schedule M
(b) Schedule N
(c) Schedule P
(d) Schedule S
• N - List of minimum equipment for efficient running of a
pharmacy.
• O - Standard for disinfectant fluid.
• P - Life period of drug.
• P₁ - Pack sizes of drugs.
25. Schedule O is related to
(a) Standard for ophthalmic preparation
(b) Standard for disinfectant fluids
(c) For external use only
(d) Standard for cosmetics
25. Schedule O is related to
(a) Standard for ophthalmic preparation
(b) Standard for disinfectant fluids
(c) For external use only
(d) Standard for cosmetics
• N - List of minimum equipment for efficient running of a
pharmacy.
• O - Standard for disinfectant fluid.
• P - Life period of drug.
• P₁ - Pack sizes of drugs.
26. Schedule P of Drugs and Cosmetics Act
refers to
(a) Provisions for disinfectants
(b) Life period of drugs
(c) Pack sizes of drugs
(d) Standards for contraceptives
26. Schedule P of Drugs and Cosmetics Act
refers to
(a) Provisions for disinfectants
(b) Life period of drugs
(c) Pack sizes of drugs
(d) Standards for contraceptives
• N - List of minimum equipment for efficient running of a
pharmacy.
• O - Standard for disinfectant fluid.
• P - Life period of drug.
• P₁ - Pack sizes of drugs.
27. The schedule in D and C act that deals with
the pack sizes of drugs is
(a) Schedule P1
(b) Schedule K
(c) Schedule R
(d) Schedule S
27. The schedule in D and C act that deals with
the pack sizes of drugs is
(a) Schedule P1
(b) Schedule K
(c) Schedule R
(d) Schedule S
• N - List of minimum equipment for efficient running of a
pharmacy.
• O - Standard for disinfectant fluid.
• P - Life period of drug.
• P₁ - Pack sizes of drugs.
28. "Rule 134 of Drugs and Cosmetics Rules"
stipulates that no cosmetic shall be imported
which contains coal tar colour other than the
one prescribed in Schedule
(a) Q
(b) N
(c) M
(d) C
28. "Rule 134 of Drugs and Cosmetics Rules"
stipulates that no cosmetic shall be imported
which contains coal tar colour other than the
one prescribed in Schedule
(a) Q
(b) N
(c) M
(d) C
• Q - List of coals tar colors permitted to be used in cosmetics.
• R - Standard for condoms made of rubber latex and other mechanical
contraceptives.
• R₁ - Standard for mechanical contraceptive.
• S-Standard for cosmetics.
• T- Good manufacturing practice for Ayurvedic Siddha, Unani medicines.
29. Schedule R of Drugs and Cosmetics Act
deals with
(a) Disinfectants
(b) Antiseptics
(c) Mechanical Contraceptives
(d) Dyes, Colours & Pigments
29. Schedule R of Drugs and Cosmetics Act
deals with
(a) Disinfectants
(b) Antiseptics
(c) Mechanical Contraceptives
(d) Dyes, Colours & Pigments
• Q - List of coals tar colors permitted to be used in cosmetics.
• R - Standard for condoms made of rubber latex and other mechanical
contraceptives.
• R₁ - Standard for mechanical contraceptive.
• S-Standard for cosmetics.
• T- Good manufacturing practice for Ayurvedic Siddha, Unani medicines.
30. Schedule "S" in Drugs and Cosmetics Act to
the rules stands for
(a) Standard for surgical dressing
(b) Standard for sterilized umbilical tapes
(c) Standard for cosmetics
(d) Standard for disinfectant fluids
30. Schedule "S" in Drugs and Cosmetics Act to
the rules stands for
(a) Standard for surgical dressing
(b) Standard for sterilized umbilical tapes
(c) Standard for cosmetics
(d) Standard for disinfectant fluids
• Q - List of coals tar colors permitted to be used in cosmetics.
• R - Standard for condoms made of rubber latex and other mechanical
contraceptives.
• R₁ - Standard for mechanical contraceptive.
• S-Standard for cosmetics.
• T- Good manufacturing practice for Ayurvedic Siddha, Unani medicines.
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31. Manufacturer of cosmetics to conform to
the latest Bureau of Indian Standards
requirements is specified in
(a) Schedule-A
(b) Schedule-S
(c) Schedule-F
(d) Schedule T
31. Manufacturer of cosmetics to conform to
the latest Bureau of Indian Standards
requirements is specified in
(a) Schedule-A
(b) Schedule-S
(c) Schedule-F
(d) Schedule T
• Q - List of coals tar colors permitted to be used in cosmetics.
• R - Standard for condoms made of rubber latex and other mechanical
contraceptives.
• R₁ - Standard for mechanical contraceptive.
• S-Standard for cosmetics.
• T- Good manufacturing practice for Ayurvedic Siddha, Unani medicines.
32. Under which Schedule "Good
Manufacturing practices of Ayurveda, Siddha
and for all Unani drugs" are described
(a) Schedule -T
(b) Schedule –S
(c) Schedule M
(d) Schedule -Z
32. Under which Schedule "Good
Manufacturing practices of Ayurveda, Siddha
and for all Unani drugs" are described
(a) Schedule -T
(b) Schedule –S
(c) Schedule M
(d) Schedule -Z
• Q - List of coals tar colors permitted to be used in cosmetics.
• R - Standard for condoms made of rubber latex and other mechanical
contraceptives.
• R₁ - Standard for mechanical contraceptive.
• S-Standard for cosmetics.
• T- Good manufacturing practice for Ayurvedic Siddha, Unani medicines.
33. Every drug manufacturer shall maintain
manufacturing and analytical records to the
Drugs and Cosmetics Rules, 1945 as per
(a) Schedule M
(b) Schedule U
(c) Schedule V
(d) Schedule T
33. Every drug manufacturer shall maintain
manufacturing and analytical records to the
Drugs and Cosmetics Rules, 1945 as per
(a) Schedule M
(b) Schedule U
(c) Schedule V
(d) Schedule T
• U- Particulars to be shown in manufacturing records.
• U₁ - Particulars to be shown in manufacturing, raw material and
analytical records of cosmetic
• V - Standard for patent or proprietary medicines.
• W - List of drug which is to be marketed under generic names only.
• X - List of drugs whose import, manufacture and sale, labeling and
packaging are governed by special provision.
• Y-Requirement and guideline for permission to import and
manufacture of new drugs for sale or to undertake clinical trial
34. What does Schedule W of Drugs and
Cosmetics Act 1940 and Rules 1945 contain
(a) List of drugs which shall be marketed under
generic name only
(b) Life period of drugs
(c) Standards for cosmetics
(d) Biological and special products
34. What does Schedule W of Drugs and
Cosmetics Act 1940 and Rules 1945 contain
(a) List of drugs which shall be marketed under
generic name only
(b) Life period of drugs
(c) Standards for cosmetics
(d) Biological and special products
• U- Particulars to be shown in manufacturing records.
• U₁ - Particulars to be shown in manufacturing, raw material and
analytical records of cosmetic
• V - Standard for patent or proprietary medicines.
• W - List of drug which is to be marketed under generic names only.
• X - List of drugs whose import, manufacture and sale, labeling and
packaging are governed by special provision.
• Y-Requirement and guideline for permission to import and
manufacture of new drugs for sale or to undertake clinical trial
35. Habit forming drugs are concerned with
(a) Schedule FF
(b) Schedule K
(c) Schedule X
(d) Schedule D
35. Habit forming drugs are concerned with
(a) Schedule FF
(b) Schedule K
(c) Schedule X
(d) Schedule D
• U- Particulars to be shown in manufacturing records.
• U₁ - Particulars to be shown in manufacturing, raw material and
analytical records of cosmetic
• V - Standard for patent or proprietary medicines.
• W - List of drug which is to be marketed under generic names only.
• X - List of drugs whose import, manufacture and sale, labeling and
packaging are governed by special provision.
• Y-Requirement and guideline for permission to import and
manufacture of new drugs for sale or to undertake clinical trial
36. List of narcotic drugs and psychotropic
substances are listed in
(a) Schedule U
(b) Schedule R
(c) Schedule W
(d) Schedule X
36. List of narcotic drugs and psychotropic
substances are listed in
(a) Schedule U
(b) Schedule R
(c) Schedule W
(d) Schedule X
• U- Particulars to be shown in manufacturing records.
• U₁ - Particulars to be shown in manufacturing, raw material and
analytical records of cosmetic
• V - Standard for patent or proprietary medicines.
• W - List of drug which is to be marketed under generic names only.
• X - List of drugs whose import, manufacture and sale, labeling and
packaging are governed by special provision.
• Y-Requirement and guideline for permission to import and
manufacture of new drugs for sale or to undertake clinical trial
37. The schedule in Drugs and Cosmetics Act
that deals with requirement and guidelines the
clinical trial import and manufacture of new
drug is
(a) Schedule O
(b) Schedule M
(c) Schedule F
(d) Schedule Y
37. The schedule in Drugs and Cosmetics Act
that deals with requirement and guidelines the
clinical trial import and manufacture of new
drug is
(a) Schedule O
(b) Schedule M
(c) Schedule F
(d) Schedule Y
• U- Particulars to be shown in manufacturing records.
• U₁ - Particulars to be shown in manufacturing, raw material and
analytical records of cosmetic
• V - Standard for patent or proprietary medicines.
• W - List of drug which is to be marketed under generic names only.
• X - List of drugs whose import, manufacture and sale, labeling and
packaging are governed by special provision.
• Y-Requirement and guideline for permission to import and
manufacture of new drugs for sale or to undertake clinical trial
38. Ibuprofen tablet belongs to schedule
(a) X
(b) G
(c) H
(d) B
38. Ibuprofen tablet belongs to schedule
(a) X
(b) G
(c) H
(d) B
Schedule H Drugs
• Acebutol HCl
• Acyclovir
• Ibuprofen
• Imipramine
• Ketamine HCl
• Ketoprofen
• Metronidazole etc.
39. Which of the following is a schedule X drug
(a) Thalidomide
(b) Amoxycillin
(c) Glutethimide
(d) Halothane
39. Which of the following is a schedule X drug
(a) Thalidomide
(b) Amoxycillin
(c) Glutethimide
(d) Halothane
Schedule H Drugs
• Amobarbital
• Amphetamine
• Barbital
• Dexamphetamine
• Glutethimide
• Methylphenidate
• Phencyclidine etc.
40. Which of the following is a Schedule G drug
(a) Heparin
(b) Labetalol HCI
(c) Barbituric acid, its salts and derivatives
(d) Hydantoin, its salts; its derivatives and their
salts
40. Which of the following is a Schedule G drug
(a) Heparin
(b) Labetalol HCI
(c) Barbituric acid, its salts and derivatives
(d) Hydantoin, its salts; its derivatives and their
salts
Schedule G Drugs
• Bleomycin
• Chlorpropamide
• Cisplatin
• Cyclophosphamide & its salts
• Doxorubicin HCl
• Ethosuximide
• Hydantoin, its salts, its derivatives etc
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