Cefuroxime Sodium
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:
Cefuroxime sodium 789mg equivalent to 750 mg cefuroxime
Disponibbli minn:
Hospira NZ Ltd
INN (Isem Internazzjonali):
Cefuroxime sodium 789 mg (equivalent to 750 mg cefuroxime)
Dożaġġ:
750 mg
Għamla farmaċewtika:
Powder for injection
Kompożizzjoni:
Active: Cefuroxime sodium 789mg equivalent to 750 mg cefuroxime
Unitajiet fil-pakkett:
Vial, glass, IV/IM - 12.6 mL x 10, 10 dose units
Klassi:
Prescription
Tip ta 'preskrizzjoni:
Prescription
Manifatturat minn:
ACS Dobfar SpA
Sommarju tal-prodott:
Package - Contents - Shelf Life: Vial, glass, IV/IM - 12.6 mL x 10 - 10 dose units - 36 months unopened stored at or below 25°C 24 hours opened stored at 2° to 8°C (Refrigerate, do not freeze) 24 hours reconstituted stored at 2° to 8°C (Refrigerate, do not freeze)
Data ta 'l-awtorizzazzjoni:
1999-09-14
