DICLAC

This brand name is authorized in Brazil, Croatia, Cyprus, Estonia, Germany, Ireland, Lithuania, Malta, Poland, Romania.

Active ingredients

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

1	Diclofenac UNII QTG126297Q - DICLOFENAC SODIUM
	Diclofenac is a non-steroidal anti-inflammatory drug. The mechanism of action of diclofenac in AK may be related to the inhibition of the cycloxygenase pathway leading to reduced prostaglandin E2 (PGE2) synthesis. In addition, immunohistochemistry (IHC) from skin biopsies ac revealed that the clinical effects of diclofenac in AK are primarily due to anti-inflammatory, anti-angiogenic and possibly anti-proliferative effects and apoptosis-inducing mechanisms.
	Read more about Diclofenac

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
DICLAC Enteric-coated tablet	MPI, EU: SmPC	Υπουργείο Υγείας (CY)
DICLAC Solution for injection	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
M01AB05	Diclofenac	M Musculo-skeletal system → M01 Antiinflammatory and antirheumatic products → M01A Antiinflammatory and antirheumatic products, non-steroids → M01AB Acetic acid derivatives and related substances
Discover more medicines within M01AB05

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	511503102110411
DE	Bundesinstitut für Arzneimittel und Medizinprodukte	03223108, 03223120, 03223166, 03223172, 03223189, 03223195, 03223203, 03223226, 03424835, 03424841, 05388026, 06339969, 06339975, 07238940, 07238957, 07238992, 07239000, 07577211, 07577228, 12605263
EE	Ravimiamet	1012307, 1040331, 1040342, 1040353, 1040364, 1071908, 1071920, 1071942, 1071964, 1071986, 1073999, 1078163, 1078174, 1153257, 1153268, 1185690, 1762679, 1762680, 1790737, 1880489
HR	Agencija za lijekove i medicinske proizvode	HR-H-663384318
IE	Health Products Regulatory Authority	20117, 22217, 22233, 22241, 22259, 22274, 34890
LT	Valstybinė vaistų kontrolės tarnyba	1002550, 1002551, 1002556, 1002557, 1002559, 1003647, 1003648, 1014204, 1014205, 1015354, 1015355, 1020218, 1020219, 1020220
MT	Medicines Authority	AA1316/00401, AA1316/00402
PL	Rejestru Produktów Leczniczych	100075118, 100079317, 100086990, 100087009, 100109870, 100109886, 100121456, 100264173, 100354338, 100387533, 100418334, 100418860, 100433730, 100436473, 100439773, 100443527, 100447318, 100450916, 100450923, 100454080, 100457310, 100463575, 100463700, 100463718, 100464702
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W06822001, W06822002, W41807001, W41807002