Conthram
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:
Dantron 5 mg/mL; Poloxamer 188 40 mg/mL
Disponibbli minn:
Pacific Pharmaceuticals Limited (part of Mylan)
INN (Isem Internazzjonali):
Dantron 5 mg/mL
Dożaġġ:
5mg/40mg/mL
Għamla farmaċewtika:
Oral suspension
Kompożizzjoni:
Active: Dantron 5 mg/mL Poloxamer 188 40 mg/mL Excipient: Aluminium magnesium silicate Citric acid peach 403788 peach N30 nipasept; sodium salts of methyl, ethyl, propyl paraben Potassium sorbate Propylene glycol alginate Purified water Saccharin sodium Sorbitol Xanthan gum
Unitajiet fil-pakkett:
Bottle, PETG 300mL, 300 mL
Klassi:
Prescription
Tip ta 'preskrizzjoni:
Prescription
Manifatturat minn:
Union Quimico Farmaceutica SA (Uquifa SA)
Sommarju tal-prodott:
Package - Contents - Shelf Life: Bottle, PETG 300mL - 300 mL - 24 months from date of manufacture stored at or below 30°C protect from light
Data ta 'l-awtorizzazzjoni:
1999-05-21
