HUMALOG

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

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 about Insulin lispro

Medication package inserts

Below package inserts are available for further reading:

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

Medicine classification

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

ATC code	Group title	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)
Country: AU	Pharmaceutical Benefits Scheme	Identifier(s): 11645X, 12234X, 12237C, 12261H, 8084L, 8212F, 8390N, 8874C
Country: BR	Câmara de Regulação do Mercado de Medicamentos	Identifier(s): 507601401157310, 507601402153319, 507601405152216, 507604102150416, 507604201159314, 507604301153210, 507604801156219, 507604901150417, 507605001153418, 507605002151419, 507605101158411
Country: CA	Health Products and Food Branch	Identifier(s): 02229704, 02229705, 02240294, 02240297, 02403412, 02403420, 02403439, 02439611, 02470152
Country: EC	Agencia Nacional de Regulación, Control y Vigilancia Sanitaria	Identifier(s): 29665-02-11, 29678-02-11
Country: EE	Ravimiamet	Identifier(s): 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
Country: ES	Centro de información online de medicamentos de la AEMPS	Identifier(s): 196007041, 196007044, 96007002, 96007031, 96007033, 96007035
Country: FI	Lääkealan turvallisuus- ja kehittämiskeskus	Identifier(s): 031088, 156495, 156506, 156517, 433086, 484224, 556964
Country: FR	Base de données publique des médicaments	Identifier(s): 61650831, 61872223, 64052173, 65132156, 65228400, 66081056, 66537912, 67759549, 69304169
Country: GB	Medicines & Healthcare Products Regulatory Agency	Identifier(s): 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
Country: HK	Department of Health Drug Office	Identifier(s): 42886, 42887, 60379, 60380, 60381
Country: IE	Health Products Regulatory Authority	Identifier(s): 41045, 41046, 69001, 69050, 69057, 69091, 69105, 69132, 69148, 69184
Country: IL	מִשְׂרַד הַבְּרִיאוּת	Identifier(s): 3323, 3436, 6628, 6629, 6630, 7998, 9164
Country: JP	医薬品医療機器総合機構	Identifier(s): 2492414A1026, 2492414A2030, 2492414A3029, 2492414A4025, 2492414G5024, 2492414G6020, 2492414G7027, 2492414G9020
Country: LT	Valstybinė vaistų kontrolės tarnyba	Identifier(s): 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
Country: NG	Registered Drug Product Database	Identifier(s): A6-0617
Country: NL	Z-Index G-Standaard	Identifier(s): 14002248, 14255340, 15027759
Country: NL	Z-Index G-Standaard, PRK	Identifier(s): 121363, 121371, 121398, 121916, 65722, 65838, 65854, 65862
Country: NZ	Medicines and Medical Devices Safety Authority	Identifier(s): 7450, 7451, 9008, 9009, 9010, 9011
Country: PL	Rejestru Produktów Leczniczych	Identifier(s): 100029325, 100029348, 100090709, 100090744, 100197420, 100197436, 100197459, 100208677, 100310453, 100417866, 100461206
Country: RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	Identifier(s): W03665001, W03665002, W12817001, W12817002, W12817003, W52601001, W52601002, W52602001, W52602002, W52605001, W53873001, W53873002, W53874001, W53874002, W53875001, W53875002, W62269001, W64009002
Country: SG	Health Sciences Authority	Identifier(s): 09533P, 11171P, 11227P, 13719P, 14025P
Country: TR	İlaç ve Tıbbi Cihaz Kurumu	Identifier(s): 8699673774152, 8699673774169, 8699673954196, 8699673954202, 8699673954226, 8699673954271, 8699673954288, 8699673954301, 8699673954516, 8699673954523, 8699673954530, 8699673954547
Country: US	FDA, National Drug Code	Identifier(s): 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
Country: ZA	Health Products Regulatory Authority	Identifier(s): 33/21.1/0073, 33/21.1/0074, 50/21.1/0680