CLENIL

This brand name is authorized in Albania, Brazil, Cyprus, Hong Kong SAR China, Ireland, Italy, Romania, Singapore, South Africa, Tunisia, UK.

Active ingredients

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

1	Beclometasone UNII 5B307S63B2 - BECLOMETHASONE DIPROPIONATE
	Beclometasone is a pro-drug with weak glucocorticoid receptor binding affinity. It is extensively hydrolysed via esterase enzymes to the active metabolite beclometasone-17-monopropionate (B-17-MP), which has potent topical anti-inflammatory activity.
	Read more about Beclometasone

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
CLENIL Pressurised inhalation solution	MPI, EU: SmPC	Medicines & Healthcare Products Regulatory Agency (GB)
CLENIL FORTE SPRAY Pressurised inhalation solution	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
R01AD01	Beclometasone	R Respiratory system → R01 Nasal preparations → R01A Decongestants and other nasal preparations for topical use → R01AD Corticosteroids
Discover more medicines within R01AD01
R03BA01	Beclometasone	R Respiratory system → R03 Drugs for obstructive airway diseases → R03B Other drugs for obstructive airway diseases, inhalants → R03BA Glucocorticoids
Discover more medicines within R03BA01

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
AL	Fondi i Sigurimit të Detyrueshëm të Kujdesit Shëndetësor	300/26
BR	Câmara de Regulação do Mercado de Medicamentos	508501103136411, 508501109177411, 508501110175419, 508503801175311, 508503803178318, 508503806177312, 508503809176317, 508503810174314, 508512070011003, 508517030011403
GB	Medicines & Healthcare Products Regulatory Agency	106179, 106184, 106194, 106197
HK	Department of Health Drug Office	64227
IT	Agenzia del Farmaco	023103068, 023103132, 028825014
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W41683001
SG	Health Sciences Authority	03597P, 13313P
TN	Direction de la Pharmacie et du Médicament	7133011, 7133012, 7133013, 7133014, 7133015
ZA	Health Products Regulatory Authority	34/21.5.1/0208