Duovent Respules
Country: New Zealand
Lingwa: Ingliż
Sors: Medsafe (Medicines Safety Authority)
Xi dokumenti għal dan il-prodott mhumiex disponibbli bħalissa, tista 'tibgħat talba lis-servizz tal-konsumatur tagħna u aħna ninnotifikawkom malli nkunu nistgħu niksbuhom.
Ibgħat talba.
Ibgħat talba.
Ingredjent attiv:
Fenoterol hydrobromide 0.3125 mg/mL; Ipratropium bromide monohydrate 0.125 mg/mL
Disponibbli minn:
Boehringer Ingelheim (NZ) Ltd
INN (Isem Internazzjonali):
Fenoterol hydrobromide 0.3125 mg/mL
Għamla farmaċewtika:
Solution for inhalation
Kompożizzjoni:
Active: Fenoterol hydrobromide 0.3125 mg/mL Ipratropium bromide monohydrate 0.125 mg/mL Excipient: Hydrochloric acid Purified water Sodium chloride
Unitajiet fil-pakkett:
Ampoule, (2 x 10) 4 mL respules, 20 dose units
Klassi:
Prescription
Tip ta 'preskrizzjoni:
Prescription
Manifatturat minn:
Boehringer Ingelheim Pharma GmbH & Co KG
Sommarju tal-prodott:
Package - Contents - Shelf Life: Ampoule, (2 x 10) 4 mL respules - 20 dose units - 24 months from date of manufacture stored at or below 25°C
Data ta 'l-awtorizzazzjoni:
1986-02-19
