Sugammadex Ireland - English - HPRA (Health Products Regulatory Authority)

sugammadex

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Sugammadex 10 mg/ml solution for injection in pre-filled syringe Ireland - English - HPRA (Health Products Regulatory Authority)

sugammadex 10 mg/ml solution for injection in pre-filled syringe

laboratoire aguettant - sugammadex sodium - solution for injection in pre-filled syringe - sugammadex

Sugammadex 100 mg/ml solution for injection Ireland - English - HPRA (Health Products Regulatory Authority)

sugammadex 100 mg/ml solution for injection

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Sugammadex 50 mg/ml solution for injection in pre-filled syringe Ireland - English - HPRA (Health Products Regulatory Authority)

sugammadex 50 mg/ml solution for injection in pre-filled syringe

laboratoire aguettant - sugammadex sodium - solution for injection in pre-filled syringe - sugammadex

Sugammadex 100 mg/mL solution for injection Ireland - English - HPRA (Health Products Regulatory Authority)

sugammadex 100 mg/ml solution for injection

msn labs europe limited - sugammadex sodium - solution for injection - sugammadex

SUGAMMADEX-DR REDDY'S sugammadex (as sodium) 200 mg/2 mL injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

sugammadex-dr reddy's 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.

SUGAMMADEX-DRLA sugammadex (as sodium) 200 mg/2 mL injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

sugammadex-drla 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.

SUGAMMADEX-DRLA sugammadex (as sodium) 500 mg/5 mL injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

sugammadex-drla 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 ACCORD sugammadex (as sodium) 500 mg/5 mL solution for injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

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

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

SUGAMMADEX VIATRIS sugammadex (as sodium) 500 mg/5 mL solution for injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

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

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