BISOLVON

This brand name is authorized in Austria, Brazil, Germany, Ecuador, Finland, France, Croatia, Ireland, Japan, Malta, Mexico, Netherlands, New Zealand, United Kingdom, South Africa

Active ingredients

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

1 Bromhexine
UNII YC2ZOM3Z8V - BROMHEXINE HYDROCHLORIDE

Bromhexine is an expectorant used in the treatment of respiratory disorders associated with viscid or excessive mucus. Bromhexine is a synthetic derivative of the herbal active ingredient vasicine. It has been shown to increase the proportion of serous bronchial secretion, making it more easily expectorated. It is indicated as “secretolytic therapy in bronchopulmonary diseases associated with abnormal mucus secretion and impaired mucus transport”.

Read about Bromhexine

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
BISOLVON Oral solution Health Products Regulatory Authority (IE) MPI, EU: SmPC

Medicine classification

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

ATC code Group title Classification
R05CB02 Bromhexine R Respiratory system → R05 Cough and cold preparations → R05C Expectorants, excl. combinations with cough suppressants → R05CB Mucolytics
Discover more medicines within R05CB02

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: BR Câmara de Regulação do Mercado de Medicamentos Identifier(s): 576720050070817, 576720050070917, 576720050071017
Country: DE Bundesinstitut für Arzneimittel und Medizinprodukte Identifier(s): 00139011, 07706855
Country: EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria Identifier(s): 4383-MEE-0918, 4481-MEE-1118, 4528-MEE-0119
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 034367, 045051, 112976, 420976
Country: FR Base de données publique des médicaments Identifier(s): 61360073
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 246171
Country: HR Agencija za lijekove i medicinske proizvode Identifier(s): HR-H-025912186, HR-H-042974735, HR-H-667277868
Country: IE Health Products Regulatory Authority Identifier(s): 15328
Country: JP 医薬品医療機器総合機構 Identifier(s): 2234001F1312, 2234400A1062, 2234700G1051
Country: MT Medicines Authority Identifier(s): MA1470/00101, PI1438/04401A, PI908/05701A
Country: MX Comisión Federal para la Protección contra Riesgos Sanitarios Identifier(s): 73688, 78884
Country: NL Z-Index G-Standaard Identifier(s): 12357782, 12515140, 13529919, 14049430
Country: NL Z-Index G-Standaard, PRK Identifier(s): 1325, 16810, 17922, 46108
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 491, 493
Country: ZA Health Products Regulatory Authority Identifier(s): C/10.1/66

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