HUMALOG

This brand name is authorized in United States. It is also authorized in Australia, Austria, Brazil, Canada, Croatia, Cyprus, Ecuador, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Japan, Lithuania, Netherlands, New Zealand, Nigeria, Poland, Romania, Singapore, South Africa, Spain, Turkey, UK.

Active ingredients

The drug HUMALOG contains one active pharmaceutical ingredient (API):

1	Insulin lispro UNII GFX7QIS1II - INSULIN LISPRO
	The primary activity of insulin lispro is the regulation of glucose metabolism.
	Read more about Insulin lispro

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
HUMALOG 100 units/ml Solution for injection in vial / Cartridge / KwikPen - Junior KwikPen	MPI, EU: SmPC	European Medicines Agency (EU)
HUMALOG Mix25 100 units/ml Suspension for injection in vial / cartridge / KwikPen pre-filled pen	MPI, EU: SmPC	European Medicines Agency (EU)
HUMALOG 200 units/ml Solution for injection KwikPen pre-filled pen	MPI, EU: SmPC	European Medicines Agency (EU)
HUMALOG Mix50 100 units/ml Suspension for injection in cartridge / KwikPen pre-filled pen	MPI, EU: SmPC	European Medicines Agency (EU)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group		Classification
A10AB04	Insulin lispro	A Alimentary tract and metabolism → A10 Drugs used in diabetes → A10A Insulins and analogues → A10AB Insulins and analogues for injection, fast-acting
Discover more medicines within A10AB04
A10AD04	Insulin lispro	A Alimentary tract and metabolism → A10 Drugs used in diabetes → A10A Insulins and analogues → A10AD Insulins and analogues for injection, intermediate-acting combined with fast-acting
Discover more medicines within A10AD04

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country	Identification scheme	Identifier(s)
AU	Pharmaceutical Benefits Scheme	11645X, 12234X, 12237C, 12261H, 8084L, 8212F, 8390N, 8874C
BR	Câmara de Regulação do Mercado de Medicamentos	507601401157310, 507601402153319, 507601405152216, 507604102150416, 507604201159314, 507604301153210, 507604801156219, 507604901150417, 507605001153418, 507605002151419, 507605101158411
CA	Health Products and Food Branch	02229704, 02229705, 02240294, 02240297, 02403412, 02403420, 02403439, 02439611, 02470152
EC	Agencia Nacional de Regulación, Control y Vigilancia Sanitaria	29665-02-11, 29678-02-11
EE	Ravimiamet	1012420, 1012431, 1040409, 1043008, 1043019, 1111284, 1213568, 1213580, 1213591, 1213995, 1214020, 1214053, 1216752, 1216763, 1216785, 1216796, 1216808, 1216853, 1216875, 1226999, 1227002, 1364510, 1364521, 1364532, 1364543, 1364554, 1364565, 1364576, 1364587, 1713248, 1713259, 1713260, 1713271, 1754681, 1754692
ES	Centro de información online de medicamentos de la AEMPS	196007041, 196007044, 96007002, 96007031, 96007033, 96007035
FI	Lääkealan turvallisuus- ja kehittämiskeskus	031088, 156495, 156506, 156517, 433086, 484224, 556964
FR	Base de données publique des médicaments	61650831, 61872223, 64052173, 65132156, 65228400, 66081056, 66537912, 67759549, 69304169
GB	Medicines & Healthcare Products Regulatory Agency	103450, 138781, 138848, 138850, 142479, 142481, 142485, 165304, 180488, 187454, 187456, 196132, 196134, 196140, 289269, 32758, 32804, 32848, 352170, 374393, 374395, 375506, 375511, 376664, 379719, 379721, 379723, 392308
HK	Department of Health Drug Office	42886, 42887, 60379, 60380, 60381
IE	Health Products Regulatory Authority	41045, 41046, 69001, 69050, 69057, 69091, 69105, 69132, 69148, 69184
IL	מִשְׂרַד הַבְּרִיאוּת	3323, 3436, 6628, 6629, 6630, 7998, 9164
JP	医薬品医療機器総合機構	2492414A1026, 2492414A2030, 2492414A3029, 2492414A4025, 2492414G5024, 2492414G6020, 2492414G7027, 2492414G9020
LT	Valstybinė vaistų kontrolės tarnyba	1004386, 1004509, 1004510, 1004662, 1005038, 1005039, 1005040, 1005172, 1028868, 1028870, 1028876, 1032128, 1032129, 1032130, 1032131, 1058362, 1075234, 1075235, 1075236, 1075237, 1084273, 1084274, 1084275, 1088015, 1088016, 1088017, 1091111, 1091112, 1091113
NG	Registered Drug Product Database	A6-0617, A6-0618
Switch country to Nigeria in order to find specific presentations of HUMALOG
NL	Z-Index G-Standaard	14002248, 14255340, 15027759
NL	Z-Index G-Standaard, PRK	121363, 121371, 121398, 121916, 65722, 65838, 65854, 65862
NZ	Medicines and Medical Devices Safety Authority	7450, 7451, 9008, 9009, 9010, 9011
PL	Rejestru Produktów Leczniczych	100029325, 100029348, 100090709, 100090744, 100197420, 100197436, 100197459, 100208677, 100310453, 100417866, 100461206
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W03665001, W03665002, W12817001, W12817002, W12817003, W52601001, W52601002, W52602001, W52602002, W52605001, W53873001, W53873002, W53874001, W53874002, W53875001, W53875002, W62269001, W64009002
SG	Health Sciences Authority	09533P, 11171P, 11227P, 13719P, 14025P
TR	İlaç ve Tıbbi Cihaz Kurumu	8699673774152, 8699673774169, 8699673954196, 8699673954202, 8699673954226, 8699673954271, 8699673954288, 8699673954301, 8699673954516, 8699673954523, 8699673954530, 8699673954547
US	FDA, National Drug Code	0002-7510, 0002-7511, 0002-7512, 0002-7516, 0002-7712, 0002-7714, 0002-8213, 0002-8797, 0002-8798, 0002-8799, 50090-1663, 50090-4488, 70518-2264
ZA	Health Products Regulatory Authority	33/21.1/0073, 33/21.1/0074, 50/21.1/0680