41.

Parkinsonism
42. Piles and Fistulae
43. Power to rejuvinate
44. Premature ageing
45. Premature greying of hair
46. Rheumatic Heart Diseases
47. Sexual Impotence, Premature ejaculation and spermatorrhoea
48. Spondylitis
49. Stammering
50. Stones in gall-bladder, kidney, bladder
51. Vericose Vein.]

SCHEDULE K
(See rule 123)

Class of Drugs Extent and Conditions of Exemption

1. Drugs falling under clause (b) (i) of Section 3
of the Drugs and Cosmetics Act, not intended for
medicinal use.
All the provisions of Chapter IV of the Act
and the Rules thereunder, subject to the
conditions that the drug is not sold for
medicinal use or for use in the manufacture of
medicines and that each container is labelled

1
[2.* * *]
2 3
[2A. Quinine and other antimalarial drugs.
4
[3.* * *]
4
[4.* * *]
5
[5. Drugs supplied by a registered medical
practitioner to his own patient or any drug
specified in Schedule C supplied by a
registered medical practitioner at the request
of another such practioner if it is specially
prepared with reference to the condition and
for the use of an individual patient provided
the registered medical practitioner is not (a)
keeping an open shop or (b) selling across the
counter or (c) engaged in the importation,
manufacture, distribution or sale of drugs in
India to a degree which render him liable to
the provisions of Chapter IV of the Act and the
rules thereunder.
409
[Persons selling the drugs by retail under
arrangements made by State Government for
sale and distribution of the drugs will be
exempted from the requirement to take out
licences for retail sale under clause (c) of
Section 18 of the Act.]
All the provisions of Chapter IV of the Act
and the Rules made thereunder, subject to the
following conditions :
5
[1. The drugs shall be purchased only from a
dealer or a manufacturer licensed under these
rules, and records of such purchases showing
the names and quantities of such drugs,
together with their batch numbers and names
and addresses of the manufacturers shall be
maintained. Such records shall be open to
inspection by an Inspector appointed under the
Act, who may, if necessary, make enquiries
about purchases of the drugs and may also take
samples for test.]
2. In the case of medicine containing a
substance specified in 6[Schedule G, H or X]
of the following additional conditions shall be
complied with:-
a. the medicine shall be labelled with the
 name and address of the registered medical
practitioner by whom it is supplied;
b. if the medicine is for external application
it shall be labelled with the words 7[***]

internal use with the dose;

c. the name of the medicine or ingredients of
the preparation and the quantities thereof,
the dose prescribed, the name of the
patient & the date of supply and the name
of the person who gave the prescription
shall be entered at the time of supply in
register to be maintained for the purpose;
d. the entry in the register shall be given a
number and that number shall be entered
on the label of the container;
e. the register and the prescription, if any, on
which the medicines are issued shall be
preserved for not less than two years from
the date of the last entry in the register or
the date of the prescription, as the case
may be.
8
[3. The drug will be stored under proper
storage conditions as directed on the label.]
9
[4. No drug shall be supplied or dispensed
after the date of expiration of potency recorded
on its container, label or wrapper or in
violation of any statement or direction
recorded on such container, label or wrapper.]
10
[5A. Drugs supplied by a hospital or The provisions of Chapter IV of the Act and
dispensary maintained or supported by the Rules thereunder which require them to be
Government or local body 11[***] covered by a sale licence, subject to the
following conditions :
(1) The dispensing and supply of drugs shall
be carried out by or under the supervision
of a qualified person;
(2) The premises where drugs are supplied or
stocked shall be open to inspection by an
Inspector appointed under the Drugs and
Cosmetics Act who can, if necessary, take
samples for test;
(3) The drugs shall be stored under proper
storage conditions.
(4) 12[The drugs shall be purchased from a
manufacturer or a dealer licensed under
these rules or received as transferred
stocks from hospital stores for distribution.
Records of such purchases or receipts shall
be maintained.]
(5) 13[No drug shall be supplied or dispensed
after the date of expiration of potency
recorded on its container, label or wrapper
410

14
[5B. Whole Human Blood IP and / or its
components stored for transfusion by a First
Referral Unit, Community Health Centre,
Primary Health Centre and a Hospital.
411
or in violation of any statement or
direction recorded on such container, label
or wrapper.]
The provisions of Chapter IV of the Act and
the rules made thereunder which require
obtaining of a licence for operation of a
Blood Ban k or processing Whole Human
Blood and / or its components, subject to the
following conditions, namely: -
(1) The First Referral Unit, Community Health
Centre, Primary Health Centre and / or any
Hospital shall be approved by the State /
Union Territory Licensing Authority after
satisfying the conditions and facilities
through inspection.
(2) The captive consumption of Whole Human
Blood IP or its components in the First
Referral Unit, Community Health Centre,
Primary Health Centre and / or any
Hospital shall not be more than 2000 units
annually.
(3) The Whole Human Blood an d / or its
components shall be procured only from
Government Blood Bank and / or Indian
Red Cross Society Blood Bank and / or
Regional Blood Transfusion Centre duly
licensed.
(4) The approval shall be valid for a period of
two years from the date of issue unless
sooner suspended or cancelled and First
Referral Unit, Community Health Centre,
Primary Health Centre and / or any
Hospital shall apply for renewal to the
State Licensing Authority three months
prior to the date of expiry of the approval.
(5) The First Referral Unit, Community Health
Centre, Primary Health Centre and / or any
Hospital shall have the following technical
staff for storage of blood or its
components:
(a) A trained Medical Officer for proper
procurement, storage and cross
matching of blood and / or its
components. He / she shall also be
responsible for identifying haemolysed
blood and ensure non-supply of date
expired blood or its components.
(b) A blood bank Technician with the
qualification and experience as
specified in Part XII B of Schedule F
or an experienced laboratory
technician trained in blood grouping
and cross matching.
 (6) The First Referral Unit, Community Health
Centre, Primary Health Centre and / or any
Hospital shall have an area of 10 sq.
metres. It shall be well lighted, clean and
preferably air- conditioned. Blood bank
refrigerator of appropriate capacity fitted
with alarm device and temperature
indicator with regular temperature
monitoring shall be provided to store blood
units between 2° C to 8° C and if the
components are proposed to be stored,

Part XII B of Schedule F shall also be

provided.
(7) The First Referral Unit, Community Health
Centre, Primary Health Centre and / or any
Hospital shall maintain records and
registers including details of procurements
of Whole Human Blood IP and / or blood
components, as required under Part XII B
Schedule F.
(8) (8) The First Referral Unit, Community
Health Centre, Primary Health Centre and /
or any Hospital shall store samples of
donors blood as well as patients sera for a
period seven days after transfusion.
15
[6.* * *]

7.Quinine Sulphate The provisions of sub-section (a) (i) of Section

18 of the Act to the following extent-
(i) the colour of the drug may be pink, owing
to its being coloured with an edible pink
colouring matter;
(ii) the B. P. tests for readily carbonisable
substances produce a yellow colour of an
intensity about four times the colour
produced with quinine sulphate
conforming to the B.P. standard;
(iii) other Cinchona alkaloids present shall not
exceed six per cent; and
(iv) the residue on incineration shall not exceed
0.14 per cent.
16
[8.* * *]
17
[9. Magnesium Sulphate The provisions of sub-clause (i) of clause (a)
of Section 18 of the Act to the following
extent:-
Chlorides present in the salt shall not
exceed 0.12 per cent in the case of the produce
prepared from sea water.]
18
[10. The following substances which are All provisions of Chapter IV of the Act and
used both as articles of food as well as drugs - the
(i) all condensed or powdered milk whether Rules thereunder
412
 pure, skimmed or malted, fortified with
vitamins and minerals or otherwise.
(ii) Farex, Oats, 19[***] and all other similar
cereal preparations whether fortified with
vitamins or otherwise excepting those for
parenteral use.
(iii) Virol, Bovril, Chicken essence and all
other similar predigested foods.
(iv) 20[Ginger, Pepper, Cumin, Cinnamon and
all other similar spices and condiments
unless they are specially labelled as
conforming to the standards in the Indian
Pharmacopoeia or the Official
Pharmacopoeia and official compendia
of drug standards prescribed under the
Act and Rules made thereunder.]
21
[11.* * *]
22
[12. Substances intended to be used for The provision of Chapter IV of the Act and
destruction of vermin or insects which cause Rules thereunder, which require them to be
disease in human beings or animals, viz. covered by a sale licence 23[subject to the
Insecticides and Disinfectants.] condition that provision of condition (17) of
Rule 65 of the Drugs and Cosmetics Rules,
1945 are complied with by the person stocking
or selling such substances.]
24
[13. The following household remedies, The provisions of Chapter IV of the Act and
namely- the Rules thereunder which require them to be
(1) 25[Aspirin tablets.] covered with a sales licence in Form 20-A
(2) 26[Paracetamol Tablets.] subject to the following conditions
(3) Analgesic Balms. (a) The drugs are sold only in a village
(4) Antacid preparations. having population of not more than one
(5) Gripe Water for use of infants. thousand persons and where there is no
(6) Inhalers, containing drugs for licensed dealer under the Drugs and Cosmetics
treatment of cold and nasal congestion. Act;
(7) Syrups, lozenges, pills and tablets for (b) The drugs do not contain any substance
cough. specified in 27[Schedules G, H or X];
(8) Liniments for external use. (c) The drugs are sold in the original
(9) Skin ointments and ointments for unopened containers of the licensed
burns. manufacturers;
(10) Absorbent cotton wool, bandages (d) When the drugs are sold under clause (a)
absorbent guaze and adhesive plaster.
(11) Castor Oil, liquid Paraffin and Epsom Form 20-B shall not apply.
Salt.
(12) Eucalyptus Oil
(13) Tincture Iodine, Tincture Benzoi n
C o. and Mercurochrome in containers
not exceeding 100 ml.
(14) Tablets of Quinine Sulphate I.P.
(15) Tablets of Iodochlorohydroxy
quinoline-250 mg.
28
[14. Mechanical Contraceptives The provisions of Chapter IV of the Act and
Rules thereunder, which require them to be
413

30
[14A. Vaginal contraceptive
containing Nonoxynol.
31
[15. Chemical contraceptive having the
following composition per tablet :
(1) DL-Norgestrel-0.30 mg.
Ethinyloestradiol-0.03 mg.
(2) Levonorgestrel-0.15 mg.
Ethinyloestradiol-0.03 mg.
(3) Centchroman-30mg.
(4) 32[Desogestrel -0.150mg.
Ethinyloestradiol 0.030mg.
(5) Levonorgestrel 0.1mg.
Ethinyloestradiol 0.02mg
33
[16. Cosmetics
34
[17. Ophthalmic ointments of the
Tetracycline group of drugs
35
[18.* * *]
36
[19. Hair Fixers, namely mucilaginous
preparations containing gums, used by men for
fixing beard.
37
[20. Radio Pharmaceuticals.
38
[21. Tablets of Chloroquine Salts.
covered by a sale licence 29[subject to the
condition that the provisions of condition (17)
of Rule 65 of the Drugs and Cosmetics Rules,
1945, are complied with by the person
stocking or selling mechanical contraceptives.]
pessaries The provisions of Chapter IV of the Act and
the Rules made thereunder which require them
to be covered by a sale licence subject to the
condition that the provisions of clause (17) of
Rule 65 of the Drugs and Cosmetics Rules,
1945 are complied with by the person stocking
or selling this contraceptive.]
The provisions of Chapter IV of the Act and
the rules made thereunder which required them
to be covered by a sale licence.]
The provisions of Chapter IV of the Act and
the Rules made thereunder, which require
them to be covered by a licence for sale
provided that the cosmetics sold, if of Indian
origin, are manufactured by licensed
manufacturers.]
Persons authorised by the Government to
distribute or sell the drugs under the National
Trachoma Control Programme shall be
exempted from the provisions of Chapter IV of
the Act and the Rules made thereunder, which
require the drugs to be covered by a sale
licence.]
The provisions of Chapter IV of the Act and
the rules thereunder.]
All the provisions of Chapter IV of the Act
and the rules made thereunder.]
The provisions of Chapter IV of the Act and
Rules thereunder, which require them to be
covered by a sale licence, provided the drug in
strip pack is sold under the Commercial
Distribution Scheme of the National Malaria
Eradication Programme and duly labelled as
414
 -
Ministry of Health and Family Welfare,
]
39
[22. Sales from restaurant cars of trains and The provisions of Chapter IV of the Act and
from coastal ships of household remedies, the rules thereunder which require them to be
which do not require the supervision of a covered by a sale licence, subject to the
qualified person for their sale. following conditions, namely -
(a) the records of purchase and sale of drugs
shall be maintained by the person in charge
of sale of such drugs, which shall be available
for inspection by an Inspector appointed under
the Act;
(b) the place where such drugs are stocked
shall be open to inspection by a n Inspector
appointed under the Act who can, if necessary,
takes samples for test.]
40
[23. Drugs supplied by ( i ) Multipurpose All The provisions of Chapter IV of the Act
Workers attached to Primary Health and Rules thereunder, which require them to
Centres/Sub- Centres, (ii) Community Health be covered by a sale licence, provided the
Volunteers under the Rural Health Scheme, drugs are supplied under the Health or Family
(iii) Nurses, Auxiliary Nurses, Midwives an d Welfare Programme of the Central or State
Lady Health Visitors attached to Urban Family Government.]
Welfare Centres/Primary Health Centres/Sub-
Centres and 41[(iv) Anganwadi Workers].
42
[24. Homoeopathic medicines supplied All the provisions of Chapter IV of the Act
by a registered Homoeopathic medical and the rules made thereunder subject to the
practitioner to his own patient or following conditions:
Homoeopathic medicines supplied by a (1) The Homoeopathic medicines shall be
registered Homoeopathic medical purchased only from a dealer or a
practitioner at the request of another such manufacturer licensed under the Drugs and
practitioner provided the registered Cosmetics Rules, 1945.
Homoeopathic medical practitioner is not (a) (2) The premises where the Homoeopathic
keeping an open shop, or (b) selling across the Medicines are stocked shall be open to
counter or, (c) engaged in the importation, inspection by an Inspector appointed under the
manufacture, distribution or sale of
Homoeopathic medicines in India to a degree test.]
which renders him liable to the provisions of
Chapter IV of the Act and the rules made
thereunder
43
[25. Preparations applied to human body for The provisions of Chapter IV of the Act and
the purpose of repelling insects like Rules thereunder which require them to be
mosquitoes. covered by a sale licence subject to the
conditions that such a product has been
manufactured under a valid drug
manufacturing licence.
44
[26. Medicated Dressing and The provisions of Chapter IV of the Act and
Bandages for First Aid. Rules thereunder which require them to be
covered by a sale licence subject to the
conditions that such a product has been
manufactured under a valid drug
manufacturing licence.]
415
45
[27. Oral Rehydration Salts (Manufactured
as per the following formula) :
Sodium chloride 3.5 g/litre.
Trisodium citrate dehydrate 2.9 g/litre
Potassium Chloride 1.5 g/ litre.
May be replaced by Sodium
bicarbonate(Sodium hydrogen Carbonate) 2.5
g/ litre, when citrate salt is not available.
46
[28. White or Yellow Petroleum Jelly
I.P. (Non-perfumed).
47
[29. Morphine Tablets
30. Whole Human Blood collected and
transfused by Centres r un by Armed Forces
Medical Services in border areas, small mid-
zonal hospitals including peripheral hospitals,
Field Ambulances, Mobile medical units and
other field medical units including blood
supply units in border, sensitive and field
areas.
416
The provisions of Chapter IV of the Act and
Rules thereunder which required them to be
covered by a sale licence, subject to the
conditions that such a product has been
manufactured under a valid drug
manufacturing Licence.]
The provisions of Chapter IV of the Act and
Rules thereunder which required them to be
covered by a sale licence, subject to the
condition that such a product has been
manufactured under a valid drug
manufacturing Licence.
The provisions of Chapter IV of the Act and
the rules made thereunder which require them
to be covered by a sale licence, subject to the
following conditions, namely: -
(i) The drug shall be supplied by the
Palliative Care Centres approved by the State
Government to terminally ill cancer patients
(ii) The drug shall be kept under the custody of
the Medical Officer in charge of the said
Centre.
(iii) The drug shall be purchased from a dealer
or a manufacturer who holds licence under
these rules and records of such purchases
showing the names and quantities together
with their batch numbers and names and
addresses of the manufacturers or dealers and
the names and addresses of the patients to
whom supplies have been made shall be
maintained. Such records shall be open to
inspection by an inspector appointed under the
Act, who may also take samples for test.
All the provisions of Chapter IV of the Act
and rules made thereunder which require them
to be covered by a licence to operate a Blood
Bank for collection, storage and processing of
whole human blood for sale or distribution
subject to the following conditions:-
(i) These Centres shall collect, process and
transfuse blood in emergent situations which
require lifesaving emergency surgeries/or
transfusion.
(ii) These Centres shall be under the active
direction and personal supervision of a
qualified Medical Officer, possessing the

48
[31. The following Homoeopathic
Medicines, namely: -
49
[(a) ***
50
(b) Homoeopathic Ointments, each
Tube]:
(i) Arnica Montana
(ii) Calendula Officinalis
(iii) Cantharis
(iv) Rhus Toxicodendron
(c) Biochemic tissue remedies in tablet forms,
in generic names only, each in 20gm. Packing
in 3X and 6X trituration-
(i) Calcarea Phosphorica
(ii) Calcarea Sulphurica
(iii) Ferum Phosphoricum
(iv) Kali Muriaticum
(v) Kali Phosphoricum
(vi) Kali Sulphuricum
(vii) Magnesium Phophoricum
(viii) Magnesia Sulphurica
(ix) Natrum Muriaticum
(x) Natrum Phophoricum
(xi) Natrum Sulphuricum
(xii) Silica
(d) Homoeopathic medicines, mentioned
below, in pills, each in 30C potency, in sealed
original packing of manufacturer of 8 gms:
(i) Arnica Montana
(ii) Aconitum Napellus
(iii) Arsenicum Album
qualifications and experiences specified in
condition (i) of rule 122-G.
(iii) Each blood unit shall be tested before use
for freedom from HIV I and II antibodies,
Hepatitis B surface antigen, malarial parasites
and other tests specified under the monograph
Indian Pharmacopoeia
(iv) These Centres shall have adequate
infrastructure facilities for storage and
transportation of blood.
(v) The blood collected and tested by such
Centres shall be transfused by the Centre itself
and may be made available for use of other
peripheral Armed Forces hospitals or Centres
during operational circumstances.]
The provisions of Chapter IV of the Act and
the rules made thereunder which require them
to be covered with a sale licence in Form 20-
C, subject to the following conditions: -
(i) These homoeopathic medicines shall be
[in 25gm. sold in the original sealed small quantity
packings of the licensed manufacturers.
(ii) These medicines may be stocked and sold
by retail of medicines licensed under rule 61.
(iii) These medicines shall be stored separately
from other allopathic drugs.
(iv) These medicines shall be purchased from
a manufacturer or a dealer licensed under these
rules.
(v) The purchase and sale records of these
medicines shall be maintained by the dealer
for minimum period of three years.
(vi) These medicines shall be labelled in
generic / pharmacopoeial names only.
417
(iv) Aloe Socotrina
(v) Apis Mellifica
(vi) Allium Cepa
(vii) Bryonia Alba
(viii) Borax
(ix) Belladonna
(x) Cantharis
(xi) Carbo Vegatabilis
(xii) Cina
(xiii) Colocythis
(xiv) Calendula Officinalis
(xv) Caulophyllum Thalictroides
(xvi) Cocculus Indicus
(xvii) Chamomilla
(xviii) Drosera Rotundifolia
(xix) Hypeicum Perforatum
(xx) Hepar Sulphur
(xxi) Ipecacuanha
(xxii) Ledum Palustre
(xxiii) Millefolium
(xxiv) Mercurius Solubilis
(xxv) Nux Vomica
(xxvi) Pulsatilla Nigricans
(xxvii) Podophyllum Peltatum
(xxviii) Plantago Major
(xxix) Rhus Toxicodendron
(xxx) Ruta Graveolens
(xxxi) Symphytum Officinalis
(xxxii) Veratrum Album
51
[(e) All biochemic and its combinations (1
to 28), in tablet forms, in sealed original
packing of the manufacture.]
52
[32. First Aid kit supplied along with motor The provisions of Chapter IV of the Act and
vehicle by the manufacturer or its distributors rules made thereunder which require them to
at the time of first sale of vehicle. be covered by a sale licence, subject to the
condition that the drug items are procured
from a manufacturer or a dealer licensed under
the rules.]
53
[33. Nicotine gum 54[and Lozenges] The provisions of Chapter IV of the Act and
containing upto 2 mg of nicotine the Rules made thereunder which require them
to be covered by a sale license subject to the
condition that such a product has been
manufactured under a valid drug
manufacturing license.]
55
[34. Production of Oxygen 93 per cent USP, The provisions of Chapter IV of the Act and
produced from air by the molecular sieve the Rules made thereunder which require them
process, by a hospital or Medical Institute for to be covered by manufacturing licence under
their captive consumption. the rules, provided that the production
facilities shall be open to inspection by an
Inspector appointed under the Act, who can, if
nece ]
418
56
[35. Homoeopathic hair oils having active The provisions of Chapter IV of the Act and
ingredients up to 3X potency only the rules made thereunder which require them
to be covered with a sale licence 57[***]
subject to the condition that such a product has
been manufactured under a valid
manufacturing licence and sold in the original
sealed packing of the licensed manufacturers.]
58
[36. Custom made devices All provisions of Chapter IV of the Act and
the rules made thereunder, subject to the
condition that the device being specifically
made in accordance with a duly qualified

under his responsibility, in accordance with

specific design characteristics and is intended
for the sole use of a particular patient and the

Explanation. Mass produced devices

which only need adoption to meet the specific
requirements of the medical practitioner or any
other professional user shall not be considered
to be custom made devices.]
1. Item 2 omitted by Government of India Notification No. F.1-56/47-D, dt. 16.1.1950).
2. Added by Notification No .F. I-2/47-D dt. 13-2-1950.
3. Amended by Notification No. F. I-22/59-D dt.. 9-4-1960.
4. Item 3 and 4 omitted by Notification No. F.I-6/62-D dt. 2-7-1969.
5. Subs. by G.S.R. 1074, dt: 19.8.1978.
6. Subs. by G.S.R. 462 (E), dt: 22.6.1982.
7. Certain words omitted by G.S.R. 462 (E), dt: 22.6.1982.
8. Ins. by G.S.R. 460 (E), dt: 20.6.1984.
9. Ins. by G.S.R. 592 (E), dt: 13.8.2008.
10. Added by notification No. F.1-22/59-D, dt: 9.4.1960.
11. Certain words omitted by G.S.R. 812 (E), dt: 14.11.1994.
12. Ins. by G.S.R. 648 (E), dt: 16.9.2002.
13. Ins. by G.S.R. 592 (E), dt: 13.8.2008.
14. Ins. by G.S.R. 909 (E), dt: 20.12.2001.
15. Item 6 omitted by G.S.R. 681 (E), dt: 5.12.1980.
16. Item 8 omitted by G.S.R.1185 (E), dt: 18.8.1964.
17. Added by notification No. F.1-19/50-D.S, dt: 30.3.1953.
18. Added by notification No. DR/Sch.Ddk/F.1-40/54-D.S., dt: 27.1.1955.
19. Omitted by G.S.R. 665 (E), dt: 6.5.1977.
20. Subs. by G.S.R. 19, dt: 15.12.1977.
21. Item 11 omitted by notification No. F.1-36/64-D (G.S.R 1188), dt: 17.8.1964.
22. Amended by notification No. F.1-20/60-D (S.O.400), dt: 24.1.1964.
23. Added by G.S.R. 926, dt: 24.6.1977.
24. Added by notification No. F.1-19/59-D, dt: 13.6.1961.
25. Subs by S.O. 2139, dt: 5.6.1972.
26. Subs. by G.S.R. 1060(E), dt: 5.9.1986.
27. Subs. by G.S.R. 462 (E), dt: 22.6.1982.
28. Added by notification No. F.1-39/61-D (S.O. 1057), dt: 23.3.1964.
29. Added by G.S.R. 926, dt: 24.6.1977.
30. Ins. by G.S.R. 784 (E), dt: 28.8.1989.
31. Subs by G.S.R. 730 (E), dt: 10.12.1991.
32. Ins. by G.S.R. 648 (E), dt: 16.9.2002.
33. Added by notification No. F.1-36/64-D (G.S.R 1183), dt: 17.8.1964.
34. Added by notification No. F.1-21/63-D (G.S.R 70), dt: 4.1.1965.
35. Item 18 is omitted by G.S.R. 1594, dt: 28.10.1976.
36. Added by S.O. 2139, dt: 5.6.1972.
37. Added by G.S.R. 926, dt: 24.6.1977.
419
38. Added by G.S.R. 697 (E), dt: 11.11.1977.
39. Ins. by G.S.R. 1241, dt: 15.9.1979.
40. Ins. by G.S.R. 540 (E), dt: 22.9.1980.
41. Ins. by G.S.R. 784 (E), dt: 28.8.1989.
42. Ins. by G.S.R. 680 (E), dt: 5.12.1980.
43. Ins. by G.S.R. 1060 (E), dt: 5.9.1989.
44. Ins. by G.S.R. 371 (E), dt: 24.3.1988.
45. Ins. by G.S.R. 677 (E), dt: 2.6.1988.
46. Ins. by G.S.R. 753 (E), dt: 4.11.1999.
47. Ins. by G.S.R. 6 (E), dt: 4.1.2001.
48. Ins. by G.S.R. 218 (E), dt: 28.3.2001.
49. Sub- , dt: 22.12.2009.
50. Subs. by G.S.R. 592 (E), dt: 13.8.2008.
51. Ins. by G.S.R. 592 (E), dt: 13.8.2008.
52. Ins. by G.S.R. 648 (E), dt: 16.9.2002.
53. Ins. by G.S.R. 549 (E), dt: 16.7.2003.
54. Ins. by G.S.R. 101 (E), dt: 18.2.2001.
55. Ins. by G.S.R. 734 (E), dt: 21.12.2005.
56. Ins. by G.S.R. 917 (E), dt: 22.12.2009.

58. Ins. By G.S.R. 890 (E), dt: 25.9.2014.

420