DIPEPTIVEN

This brand name is authorized in Austria, Brazil, Croatia, Ecuador, Estonia, Finland, France, Hong Kong SAR China, Ireland, Lithuania, New Zealand, Poland, Romania, Singapore, Spain, Turkey, UK.

Active ingredients

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

1	Alanine glutamine dipeptide UNII U5JDO2770Z - ALANYL GLUTAMINE
	N(2)-L-alanyl-L-glutamine is rapidly split into alanine and glutamine after infusion, which are useful amino acids for the body in dealing with hypercatabolic and/or hypermetabolic conditions.
	Read more about Alanine glutamine dipeptide

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
DIPEPTIVEN Concentrate for solution for infusion	MPI, EU: SmPC	Health Products Regulatory Authority (IE)

Medicine classification

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

ATC Group		Classification
B05XB02	Alanyl glutamine	B Blood and blood forming organs → B05 Blood substitutes and perfusion solutions → B05X I.V. solution additives → B05XB Amino acids
Discover more medicines within B05XB02

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	509503301154418, 509503302150319, 509515080029503, 509515080029603
EC	Agencia Nacional de Regulación, Control y Vigilancia Sanitaria	30045-11-11
EE	Ravimiamet	1012846, 1085251, 1668270, 1668281
ES	Centro de información online de medicamentos de la AEMPS	61771
FI	Lääkealan turvallisuus- ja kehittämiskeskus	166934, 167304
FR	Base de données publique des médicaments	67704314
GB	Medicines & Healthcare Products Regulatory Agency	308365, 308367, 75215, 78414
HK	Department of Health Drug Office	49615
HR	Agencija za lijekove i medicinske proizvode	HR-H-685461599
LT	Valstybinė vaistų kontrolės tarnyba	1007516, 1010615, 1072171, 1086455, 1089315
NZ	Medicines and Medical Devices Safety Authority	11675
PL	Rejestru Produktów Leczniczych	100077330, 100437260, 100447838, 100455979, 100462976
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W10043001, W10043002
SG	Health Sciences Authority	11183P
TR	İlaç ve Tıbbi Cihaz Kurumu	8699630768101