Sugammadex Fresenius Kabi Union européenne - anglais - EMA (European Medicines Agency)

sugammadex fresenius kabi

fresenius kabi deutschland gmbh - sugammadex sodium - neuromuscular blockade - all other therapeutic products - reversal of neuromuscular blockade induced by rocuronium or vecuronium in adults.for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

Sugammadex Amomed Union européenne - anglais - EMA (European Medicines Agency)

sugammadex amomed

aop orphan pharmaceuticals gmbh - sugammadex sodium - neuromuscular blockade - all other therapeutic products - reversal of neuromuscular blockade induced by rocuronium or vecuronium.for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

Sugammadex Adroiq Union européenne - anglais - EMA (European Medicines Agency)

sugammadex adroiq

extrovis eu ltd. - sugammadex sodium - neuromuscular blockade - all other therapeutic products - reversal of neuromuscular blockade induced by rocuronium or vecuronium in adults.for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

SUGAMMADEX ARX sugammadex (as sodium) 500 mg/5 mL solution for injection vial Australie - anglais - Department of Health (Therapeutic Goods Administration)

sugammadex arx sugammadex (as sodium) 500 mg/5 ml solution for injection vial

accelagen pty ltd - sugammadex sodium, quantity: 554 mg (equivalent: sugammadex, qty 500 mg) - injection, solution - excipient ingredients: sodium hydroxide; hydrochloric acid; water for injections - sugammadex arx is indicated for the reversal of neuromuscular blockade induced by rocuronium or vecuronium.

SUGAMMADEX ARX sugammadex (as sodium) 200 mg/2 mL solution for injection vial Australie - anglais - Department of Health (Therapeutic Goods Administration)

sugammadex arx sugammadex (as sodium) 200 mg/2 ml solution for injection vial

accelagen pty ltd - sugammadex sodium, quantity: 217.6 mg (equivalent: sugammadex, qty 200 mg) - injection, solution - excipient ingredients: sodium hydroxide; hydrochloric acid; water for injections - sugammadex arx is indicated for the reversal of neuromuscular blockade induced by rocuronium or vecuronium.

SUGAMMADEX SANDOZ sugammadex (as sodium) 500 mg/5 mL solution for injection vial Australie - anglais - Department of Health (Therapeutic Goods Administration)

sugammadex sandoz sugammadex (as sodium) 500 mg/5 ml solution for injection vial

sandoz pty ltd - sugammadex sodium, quantity: 544 mg (equivalent: sugammadex, qty 500 mg) - injection, solution - excipient ingredients: water for injections; sodium hydroxide; hydrochloric acid - reversal of neuromuscular blockade induced by rocuronium or vecuronium in patients 2 years of age and older.

SUGAMMADEX SANDOZ sugammadex (as sodium) 200 mg/2 mL solution for injection vial Australie - anglais - Department of Health (Therapeutic Goods Administration)

sugammadex sandoz sugammadex (as sodium) 200 mg/2 ml solution for injection vial

sandoz pty ltd - sugammadex sodium, quantity: 217.6 mg (equivalent: sugammadex, qty 200 mg) - injection, solution - excipient ingredients: water for injections; sodium hydroxide; hydrochloric acid - reversal of neuromuscular blockade induced by rocuronium or vecuronium in patients 2 years of age and older.

Sugammadex 100 mg/ml Solution for Injection Irlande - anglais - HPRA (Health Products Regulatory Authority)

sugammadex 100 mg/ml solution for injection

baxter holding b.v. - sugammadex sodium - solution for injection - sugammadex

SUGAMMADEX-RZ sugammadex (as sodium) 500 mg/5 mL injection vial Australie - anglais - Department of Health (Therapeutic Goods Administration)

sugammadex-rz sugammadex (as sodium) 500 mg/5 ml injection vial

dr reddys laboratories australia pty ltd - sugammadex sodium, quantity: 544 mg (equivalent: sugammadex, qty 500 mg) - injection, solution - excipient ingredients: water for injections; hydrochloric acid; sodium hydroxide - reversal of neuromuscular blockade induced by rocuronium or vecuronium in patients 2 years of age and older.

SUGAMMADEX-RZ sugammadex (as sodium) 200 mg/2 mL injection vial Australie - anglais - Department of Health (Therapeutic Goods Administration)

sugammadex-rz sugammadex (as sodium) 200 mg/2 ml injection vial

dr reddys laboratories australia pty ltd - sugammadex sodium, quantity: 217.6 mg (equivalent: sugammadex, qty 200 mg) - injection, solution - excipient ingredients: water for injections; sodium hydroxide; hydrochloric acid - reversal of neuromuscular blockade induced by rocuronium or vecuronium in patients 2 years of age and older.