LANTUS

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

Active ingredients

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

1	Insulin glargine UNII 2ZM8CX04RZ - INSULIN GLARGINE
	Insulin glargine is a human insulin analogue designed to have a low solubility at neutral pH. After injection, the acidic solution is neutralised leading to formation of a precipitate from which small amounts of insulin glargine are continuously released.
	Read more about Insulin glargine

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
LANTUS Solution for injection	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
A10AE04	Insulin glargine	A Alimentary tract and metabolism → A10 Drugs used in diabetes → A10A Insulins and analogues → A10AE Insulins and analogues for injection, long-acting
Discover more medicines within A10AE04

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
BR	Câmara de Regulação do Mercado de Medicamentos	576720050069317, 576720050069417, 576720050069517, 576720050069617
CA	Health Products and Food Branch	02245689, 02251930, 02294338
EC	Agencia Nacional de Regulación, Control y Vigilancia Sanitaria	24.489-05-02
EE	Ravimiamet	1061288, 1061299, 1061301, 1061312, 1061323, 1061334, 1061345, 1083383, 1083394, 1195781, 1195792, 1195804, 1195815, 1214109, 1214110, 1214121, 1214132, 1214154, 1214165, 1214176, 1227529, 1265688, 1265699, 1265701, 1265712, 1265723, 1265734, 1265745, 1265756, 1265767, 1265778, 1265789, 1265790, 1265802, 1265813, 1265824, 1265835
ES	Centro de información online de medicamentos de la AEMPS	00134006, 00134012, 00134033
FI	Lääkealan turvallisuus- ja kehittämiskeskus	078623, 089953, 090456, 371722
FR	Base de données publique des médicaments	61404477, 64745003, 65979151
GB	Medicines & Healthcare Products Regulatory Agency	119331, 147595, 147627, 32845, 32882, 376723, 376727, 381450, 381452, 381454
HK	Department of Health Drug Office	50530, 56520
IE	Health Products Regulatory Authority	26953, 69158, 69207, 69252, 69277
IL	מִשְׂרַד הַבְּרִיאוּת	4643, 4978
IT	Agenzia del Farmaco	035724018, 035724020, 035724032, 035724044, 035724057, 035724069, 035724071, 035724083, 035724095, 035724107, 035724119, 035724121, 035724133, 035724145, 035724158, 035724160, 035724172, 035724184, 035724196, 035724208, 035724210, 035724222, 035724234, 035724246, 035724259, 035724261, 035724273, 035724285
JP	医薬品医療機器総合機構	2492416A1033, 2492416A3036, 2492416G2024, 2492416G3020
LT	Valstybinė vaistų kontrolės tarnyba	1004370, 1004371, 1004814, 1007795, 1009237, 1010642, 1029358, 1029359, 1029360, 1029361, 1029362, 1029363, 1029364, 1029365, 1029366, 1029367, 1029368, 1029369, 1029370, 1029371, 1029372, 1029373, 1029374, 1029375, 1029376, 1029377, 1029378, 1029379, 1029380, 1029381, 1029382, 1029383, 1029384, 1029385, 1029386, 1029387, 1029388
NG	Registered Drug Product Database	A6-0109, A6-0110, A6-0139
Switch country to Nigeria in order to find specific presentations of LANTUS
NL	Z-Index G-Standaard	14710110, 14710129
NL	Z-Index G-Standaard, PRK	69086
NZ	Medicines and Medical Devices Safety Authority	13001, 8933
PL	Rejestru Produktów Leczniczych	100130515
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W08054001, W08054002, W08054003, W08054004, W08054005, W08054006, W08054007, W08054008, W10010001, W10010002, W10010003, W10010004, W10010005, W52628005, W52628006, W52628007, W52628008, W52628009, W52628010, W52628011, W52628012
SG	Health Sciences Authority	11934P, 13426P
TN	Direction de la Pharmacie et du Médicament	1823021, 1823025
TR	İlaç ve Tıbbi Cihaz Kurumu	8699809760653, 8699809950627, 8699809950634
US	FDA, National Drug Code	0088-2219, 0088-2220, 0088-5020, 0088-5021, 50090-0876, 70518-1865
ZA	Health Products Regulatory Authority	34/21.1/0248, 34/21.1/0249, 34/21.1/0250