DUKORAL

This brand name is authorized in Austria, Canada, Croatia, Estonia, Finland, France, Hong Kong SAR China, Ireland, Lithuania, Netherlands, New Zealand, Poland, Singapore, South Africa, Spain, UK.

Active ingredients

The drug DUKORAL contains a combination of these active pharmaceutical ingredients (APIs):

`1`	VIBRIO CHOLERAE INABA 48 CLASSICAL BIOTYPE, HEAT INACTIVATED UNII `4M0784008H` - VIBRIO CHOLERAE
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`2`	VIBRIO CHOLERAE INABA 6973 EL TOR BIOTYPE, FORMALIN INACTIVATED UNII `4M0784008H` - VIBRIO CHOLERAE
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`3`	VIBRIO CHOLERAE OGAWA 50 CLASSICAL BIOTYPE, FORMALIN INACTIVATED UNII `4M0784008H` - VIBRIO CHOLERAE
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`4`	VIBRIO CHOLERAE OGAWA 50 CLASSICAL BIOTYPE, HEAT INACTIVATED UNII `4M0784008H` - VIBRIO CHOLERAE
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`5`	Cholera toxin B subunit (rCTB), recombinant UNII `1FKD81GIZJ` - CHOLERA ENTEROTOXIN SUBUNIT B

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
DUKORAL Oral suspension / Granules	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
J07AE01	Cholera, inactivated, whole cell	J Antiinfectives for systemic use → J07 Vaccines → J07A Bacterial vaccines → J07AE Cholera vaccines
Discover more medicines within J07AE01

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
CA	Health Products and Food Branch	02247208
EE	Ravimiamet	1009785, 1062964, 1062975
ES	Centro de información online de medicamentos de la AEMPS	03263002
FI	Lääkealan turvallisuus- ja kehittämiskeskus	398719, 444109
FR	Base de données publique des médicaments	66974680
GB	Medicines & Healthcare Products Regulatory Agency	51860
HK	Department of Health Drug Office	58519, 63012
LT	Valstybinė vaistų kontrolės tarnyba	1027896, 1027897, 1027898
NL	Z-Index G-Standaard, PRK	79596
NZ	Medicines and Medical Devices Safety Authority	10229
PL	Rejestru Produktów Leczniczych	100148596
SG	Health Sciences Authority	12186P
ZA	Health Products Regulatory Authority	36/30.1/0129

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