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Sugammadex Lorien

Active substance: sugammadex

sugammadex sodium

Centralised EU authorisationActive

Marketing holder: LABORATORIOS LORIEN, S.L

Verified 2026-10-09 · EMA

Analogues in other countries
Composition
Analogues by country

Products with the same active substance registered in other countries.

CountryProducts
US 44
  • BRIDION
    INJECTION, SOLUTION · SUGAMMADEX SODIUM 100 mg/mL
    84549-423
    ProPharma Distribution
  • BRIDION
    INJECTION, SOLUTION · SUGAMMADEX SODIUM 100 mg/mL
    0006-5425
    Merck Sharp & Dohme LLC
  • BRIDION
    INJECTION, SOLUTION · SUGAMMADEX SODIUM 100 mg/mL
    71872-7187
    Medical Purchasing Solutions, LLC
  • BRIDION
    INJECTION, SOLUTION · SUGAMMADEX SODIUM 100 mg/mL
    0006-5423
    Merck Sharp & Dohme LLC
  • SUGAMMADEX SODIUM
    SOLUTION · SUGAMMADEX SODIUM 500 mg/5mL
    82449-242
    STERISCIENCE SPECIALTIES PRIVATE LIMITED
All products in this country (44)
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-2b19-7c7b-a46d-69ec47b919f5,01a1208c-3099-7449-9b38-72d02a0caeb2,01a1208c-3dcf-722e-87f8-a6319b9a9a9a,01a1208c-8796-79d5-8114-10213f312eda,01a1208c-9f49-7bc5-8ff9-c1356b503d77;count=44 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
EMEA/H/C/006115
Registration status
Active
ATC code
V03AB35
Sources
  • product · EMA · EMEA/H/C/006115 · Verified 2026-10-09
  • registration_status · EMA · EMEA/H/C/006115 · Verified 2026-10-09
  • ingredients.0 · EMA · EMEA/H/C/006115 · Verified 2026-10-09