KIOVIG

This brand name is authorized in Austria, Brazil, Croatia, Cyprus, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Italy, Lithuania, Netherlands, Poland, Romania, Singapore, Spain, Tunisia, Turkey, UK.

Active ingredients

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

1	Immunoglobulins, normal human, IV
	Human normal immunoglobulin contains mainly immunoglobulin G (IgG) with a broad spectrum of antibodies against infectious agents. The mechanism of action in indications other than replacement therapy is not fully elucidated, but includes immunomodulatory effects.
	Read more about Immunoglobulins, normal human, IV

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
KIOVIG Solution for infusion	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
J06BA02	Immunoglobulins, normal human, for intravascular adm.	J Antiinfectives for systemic use → J06 Immune sera and immunoglobulins → J06B Immunoglobulins → J06BA Immunoglobulins, normal human
Discover more medicines within J06BA02

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	501121010032217, 501121010032317, 501121010032417, 501121010032517, 501121010032617, 540218090001417, 540218090001517
EE	Ravimiamet	1235449, 1235450, 1235461, 1235472, 1235483, 1476996
ES	Centro de información online de medicamentos de la AEMPS	05329003, 05329004, 05329005
FI	Lääkealan turvallisuus- ja kehittämiskeskus	049902, 049913, 049925, 049936, 049947, 562577
FR	Base de données publique des médicaments	67898029
GB	Medicines & Healthcare Products Regulatory Agency	171719, 171721, 171723, 171726, 171728, 332216
HK	Department of Health Drug Office	56576
IL	מִשְׂרַד הַבְּרִיאוּת	7133, 7134
IT	Agenzia del Farmaco	037107012, 037107024, 037107036, 037107048, 037107051, 037107063
LT	Valstybinė vaistų kontrolės tarnyba	1029326, 1029327, 1029328, 1029329, 1029330, 1056101
NL	Z-Index G-Standaard, PRK	80039, 80047, 80055, 80063, 80071, 94242
PL	Rejestru Produktów Leczniczych	100155403
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W66549001, W66549002, W66549003, W66549004, W66549005
SG	Health Sciences Authority	13809P
TN	Direction de la Pharmacie et du Médicament	10623061H, 10623062H
TR	İlaç ve Tıbbi Cihaz Kurumu	8681429550172, 8681429550189, 8681429550196, 8681429550202, 8681429550219