SOLUTION CONTAINS in Croatian translation

• otopina sadrži
• otopine sadrži

Examples of using Solution contains in English and their translations into Croatian

Each 4.0 mL vial of solution contains 40.6 mg(10.2 mg/mL)
Svaka bočica od 4, 0 mL otopine sadrži 40, 6 mg(10, 2 mg/mL)

After reconstitution with 20 ml solvent, the solution contains approximately 50 mg/ml of human alpha1-proteinase inhibitor.
Nakon rekonstitucije s 20 ml otapala, otopina sadrži približno 50 mg/ml ljudskog inhibitora alfa1-proteinaze.

One pre-filled syringe of 3 ml solution contains 3 mg of ibandronic acid as sodium monohydrate.
Jedna napunjena štrcaljka s 3 ml otopine sadrži 3 mg ibandronatne kiseline u obliku natrijeva hidrata.

After reconstitution, the solution contains 40 units(approximately 1.0 mg)
Nakon rekonstitucije otopina sadrži 40 jedinica(približno 1, 0 mg) imigluceraze po ml

each ml of solution contains 10 mg cabazitaxel.
jedan ml otopine sadrži 10 mg kabazitaksela.

After reconstitution, the solution contains 5 mg of alglucosidase alfa per ml
Nakon pripreme za primjenu, otopina sadrži 5 mg alglukozidaze alfa/ml, a nakon razrjeđivanja koncentracija

After reconstitution, a deliverable volume of 0.5 ml solution contains 250 micrograms of romiplostim 500 micrograms/ml.
Nakon pripreme, korisni volumen od 0, 5 ml otopine sadrži 250 mikrograma romiplostima 500 mikrograma/ml.

After reconstitution, the solution contains 5 mg of alglucosidase alfa* per ml
Nakon rekonstitucije otopina sadrži 5 mg alglukozidaze alfa* po ml,

After reconstitution, a deliverable volume of 0.5 ml solution contains 250 µg of romiplostim 500 µg/ml.
Nakon rekonstitucije, korisni volume od 0, 5 ml otopine sadrži 250 µg romiplostima 500 µg/ml.

after reconstitution with 2.5 ml of water for injections the solution contains 400 IU/ml of albutrepenonacog alfa.
nakon rekonstitucije s 2, 5 ml vode za injekcije, otopina sadrži 400 IU/ml albutrepenonakoga alfa.

Each 2.5 mL vial contains 200 mg defibrotide and each mL solution contains 80 mg defibrotide.
Jedna bočica od 2, 5 mL sadrži 200 mg defibrotida, a jedan mL otopine sadrži 80 mg defibrotida.

After reconstitution with 14 ml water for injections, the solution contains 150 U conestat alfa per ml.
Nakon rekonstitucije s 14 ml vode za injekcije otopina sadrži 150 U konestata alfa po ml.

Do not use this medicine if you notice that the vial is damaged or the solution contains particulate matter or appears discoloured.
Ne koristite ovaj lijek ako primijetite da je bočica oštećena ili da otopina sadrži čestice ili je promijenila boju.

After dissolving, a deliverable amount of 1 ml solution contains 500 micrograms of romiplostim 500 micrograms/ml.
Nakon otapanja, korisni volumen od 1 ml otopine, sadrži 500 mikrograma romiplostima 500 mikrograma/ml.

IronPort solution contains redundant devices for monitoring all e-mails, which, besides reduced amount of spam messages,
IronPort rješenje sadržava redundantne uređaje koji nadgledaju svee- mail poruke,

The infusion solution contains approximately 1.5 mg/mL isavuconazonium sulfate corresponding to approximately 0.8 mg isavuconazole per mL.
Infuzijska otopina sadrţi pribliţno 1, 5 mg/ml izavukonazonijevog sulfata što odgovara pribliţno 0, 8 mg izavukonazola po mL.

This solution contains glucose and sodium,
Ova otopina sadrži glukozu i natrij,

Each vial of 5 ml solution contains: 1 g of human plasma protein Each vial of 10 ml solution contains: 2 g of human plasma protein Each vial of 20 ml solution contains: 4 g of human plasma protein Each vial of 50 ml solution contains: 10 g of human plasma protein.
Svaka bočica od 5 ml otopine sadržava: 1 g proteina ljudske plazme Svaka bočica od 10 ml otopine sadržava: 2 g proteina ljudske plazme Svaka bočica od 20 ml otopine sadržava: 4 g proteina ljudske plazme Svaka bočica od 50 ml otopine sadržava: 10 g proteina ljudske plazme.

which is particularly noteworthy since the new 512GB eUFS solution contains twice the number of cells compared to a 256GB eUFS.
što je posebno važno jer novo 512 GB eUFS rješenje sadrži dvostruko više stanica u usporedbi s 256 GB eUFS.

TRISENOX must be diluted with a solution containing glucose or a solution containing sodium chloride.
TRISENOX se mora razrijediti s otopinom koja sadrži glukozu ili natrijev klorid.