DEPAKINE-CHRONO

This brand name is authorized in Austria, Croatia, Cyprus, Estonia, France, Lithuania, Poland, Romania, Spain, Tunisia.

Active ingredients

The drug DEPAKINE-CHRONO contains a combination of these active pharmaceutical ingredients (APIs):

1	Sodium valproate UNII 5VOM6GYJ0D - VALPROATE SODIUM
	Valproic acid is anti-convulsant. The most likely mode of action for valproate is potentiation of the inhibitory action of gamma amino butyric acid (GABA) through an action on the further synthesis or further metabolism of GABA.
	Read more about Valproic acid
2	Valproic acid UNII 614OI1Z5WI - VALPROIC ACID
	Valproic acid is anti-convulsant. The most likely mode of action for valproate is potentiation of the inhibitory action of gamma amino butyric acid (GABA) through an action on the further synthesis or further metabolism of GABA.
	Read more about Valproic acid

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
DEPAKINE CHRONO Prolonged-release tablet	MPI, EU: SmPC	Υπουργείο Υγείας (CY)

Medicine classification

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

ATC Group		Classification
N03AG01	Valproic acid	N Nervous system → N03 Antiepileptics → N03A Antiepileptics → N03AG Fatty acid derivatives
Discover more medicines within N03AG01

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
EE	Ravimiamet	1086544, 1086555, 1836109
ES	Centro de información online de medicamentos de la AEMPS	419721021-06-2011, 60350, 60351
FR	Base de données publique des médicaments	61358994
HR	Agencija za lijekove i medicinske proizvode	HR-H-132091526, HR-H-202764510
LT	Valstybinė vaistų kontrolės tarnyba	1000566, 1007961, 1021567, 1021568, 1021569, 1021570, 1021571, 1021572, 1021573, 1021574
PL	Rejestru Produktów Leczniczych	100017799, 100156242, 100156259, 100156992, 100157017, 100157030, 100247602, 100337392, 100348415, 100375234
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W64666001, W64667001
TN	Direction de la Pharmacie et du Médicament	6260054, 9263281