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
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 FORTE SPRAY Pressurised inhalation solution MPI, EU: SmPC Υπουργείο Υγείας (CY)
 CLENIL Pressurised inhalation solution MPI, EU: SmPC Medicines & Healthcare Products Regulatory Agency (GB)

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

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