1. International Nonproprietary Names (INN) should be distinctive in sound and spelling. They should not be inconveniently long and should not be liable to confusion with names in common use.
2. The INN for a substance belonging to a group of pharmacologically related substances should, where appropriate, show this relationship. Names that are likely to convey to a patient an anatomical, physiological, pathological or therapeutic suggestion should be avoided.
These primary principles are to be implemented by using the following secondary principles:
3. In devising the INN of the first substance in a new pharmacological group, consideration should be given to the possibility of devising suitable INN for related substances, belonging to the new group.
4. In devising INN for acids, one-word names are preferred; their salts should be named without modifying the acid name, e.g. “oxacillin” and “oxacillin sodium”, “ibufenac” and “ibufenac sodium”.
5. INN for substances which are used as salts should in general apply to the active base or the active acid. Names for different salts or esters of the same active substance should differ only in respect of the name of the inactive acid or the inactive base.
For quaternary ammonium substances, the cation and anion should be named appropriately as separate components of a quaternary substance and not in the amine-salt style.
6. The use of an isolated letter or number should be avoided; hyphenated construction is also undesirable.
7. To facilitate the translation and pronunciation of INN, “f” should be used instead of “ph”, “t” instead of “th”, “e” instead of “ae” or “oe”, and “i” instead of “y”; the use of the letters “h” and “k” should be avoided.
When devising an INN it is important to be aware of possible language problems . Since the name is used worldwide, not only should certain letters be avoided, but experts need to be aware of unsuitable connotations in the major languages spoken in the world.
8. Provided that the names suggested are in accordance with these principles, names proposed by the person discovering or first developing and marketing a pharmaceutical preparation, or names already officially in use in any country, should receive preferential consideration.
9. Group relationship in INN (see Guiding Principle 2) should if possible be shown by using a common stem. The following list contains examples of stems for groups of substances, particularly for new groups. There are many other stems in active use.1 Where a stem is shown without any hyphens it may be used anywhere in the name.
1 An extensive listing of stems is contained in the working document WHO/PHARM S/NOM15 which is regularly updated and can be requested from the INN Secretariat, WHO, Geneva.
Latin |
English |
|
-acum |
-ac |
anti-inflammatory agents of the ibufenac group |
-actidum |
-actide |
synthetic polypeptides with a corticotropin-like action |
-adolum |
-adol } |
analgesics |
-adol- |
-adol-} |
analgesics |
-astum |
-ast |
antiasthmatic, antiallergic substances not acting primarily as antihistaminics |
-astinum |
-astine |
antihistaminics |
-azepamum |
-azepam |
diazepam derivatives |
-bactamum |
-bactam |
b-lactamase inhibitors |
bol |
bol |
steroids, anabolic |
-buzonum |
-buzone |
anti-inflammatory analgesics, phenylbutazone derivatives |
-cain- |
-cain- |
antifibrillant substances with local anaesthetic activity |
-cainum |
-caine |
local anaesthetics |
cef- |
cef- |
antibiotics, cefalosporanic acid derivatives |
-cillinum |
-cillin |
antibiotics, derivatives of 6-amino- penicillanic acid |
-conazolum |
-conazole |
Systemic antifungal agents, miconazole derivatives |
cort |
cort |
corticosteroids, except prednisolone derivatives |
-dipinum |
-dipine |
calcium channel blockers, nifedipine derivatives |
fibratum |
-fibrate |
clofibrate derivatives |
gest |
gest |
steroids, progestogens |
gli- |
gli- |
sulfonamide hypoglycaemics |
io- |
io- |
iodine-containing contrast media |
-ium |
-ium |
quaternary ammonium compounds |
-metacinum |
-metacin |
anti-inflammatory substances, indometacin derivatives |
-mycinum |
-mycin |
antibiotics, produced by Streptomyces strains |
-nidazolum |
-nidazole |
antiprotozoal substances, metronidazole derivatives |
-ololum |
-olol |
b-adrenoreceptor antagonists |
-oxacinum |
-oxacin |
antibacterial agents, nalidixic acid derivatives |
-pridum |
-pride |
sulpiride derivatives |
-pril(at)um |
-pril(at) |
angiotensin-converting enzyme inhibitors |
-profenum |
-profen |
anti-inflammatory substances, ibuprofen derivatives |
prost |
prost |
prostaglandins |
-relinum |
-relin |
hypophyseal hormone release-stimulating peptides |
-terolum |
-terol |
bronchodilators, phenethylamine derivatives |
-tidinum |
-tidine |
histamine H2-receptor antagonists |
-trexatum |
-trexate |
folic acid antagonists |
-verinum |
-verine |
spasmolytics with a papaverine-like action |
vin- |
vin- ) |
vinca alkaloids |
-vin- |
-vin- ) |
vinca alkaloids |