AMOKSIKLAV®

Powder for solution for injection, 1000 mg + 200 mg
HospitalActive license

Active substance (INN)

amoxicillinclavulanic acid

Pharmaceutical form

Pharmaceutical formPowder for solution for injection
Strength1000 mg + 200 mg
Packagingukupno 5 staklenih bočica sa praškom za rastvor za injekciju u kartonskoj kutiji
ManufacturerLek farmacevtska družba d.d., Slovenia
Therapeutic groupAnti-infectives for systemic use (J01CR02)
Marketing authorization holderDRUŠTVO ZA TRGOVINU NA VELIKO FARMACEUTSKIM PROIZVODIMA "GLOSARIJ" D.O.O.-PODGORICA
Authorization dateJanuary 28, 2013

Analogs in Montenegro

20

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Source: CInMED register