This brand name is authorized in Australia, Austria, Brazil, Canada, Estonia, Finland, France, Hong Kong SAR China, Ireland, Japan, Malta, Netherlands, New Zealand, Tunisia, Turkey, UK.
The drug BRICANYL contains one active pharmaceutical ingredient (API):
1
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UNII
576PU70Y8E - TERBUTALINE SULFATE
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Terbutaline is a selective beta2-adrenoceptor agonist, thus producing relaxation of bronchial smooth muscle, inhibition of the release of endogenous spasmogens, inhibitions of oedema caused by endogenous mediators, increased mucociliary clearance and relaxation of the uterine muscle. |
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Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| BRICANYL Tablet | MPI, EU: SmPC | Medicines & Healthcare Products Regulatory Agency (GB) | |
| BRICANYL Solution for injection or infusion | MPI, EU: SmPC | Medicines & Healthcare Products Regulatory Agency (GB) | |
| BRICANYL TURBOHALER Inhalation powder | MPI, EU: SmPC | Medicines & Healthcare Products Regulatory Agency (GB) |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| R03AC03 | Terbutaline | R Respiratory system → R03 Drugs for obstructive airway diseases → R03A Adrenergics, inhalants → R03AC Selective beta-2-adrenoreceptor agonists |
| R03CC03 | Terbutaline | R Respiratory system → R03 Drugs for obstructive airway diseases → R03C Adrenergics for systemic use → R03CC Selective beta-2-adrenoreceptor agonists |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| AU | Pharmaceutical Benefits Scheme | 1034K, 12267P, 2817G |
| BR | Câmara de Regulação do Mercado de Medicamentos | 502300801139315, 502300901133319 |
| CA | Health Products and Food Branch | 00786616 |
| EE | Ravimiamet | 1225145, 1628793, 1734724, 1751026, 1781906 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 068001, 379698 |
| FR | Base de données publique des médicaments | 60961427, 62600742, 68242177 |
| GB | Medicines & Healthcare Products Regulatory Agency | 138379, 26851, 26858, 28294, 299801, 36340, 365069, 375768, 377581, 393592 |
| HK | Department of Health Drug Office | 19618, 30992 |
| IE | Health Products Regulatory Authority | 15458, 37420, 76408 |
| JP | 医薬品医療機器総合機構 | 2252003F1085, 2252003Q1035, 2252401A1030 |
| MT | Medicines Authority | AA227/00903 |
| NL | Z-Index G-Standaard | 13777785, 15685586 |
| NL | Z-Index G-Standaard, PRK | 152013, 152021 |
| NZ | Medicines and Medical Devices Safety Authority | 1302 |
| TN | Direction de la Pharmacie et du Médicament | 5100012, 5100016, 5100017H, 5100018, 5100019 |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8699786010406 |
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