SUGAMMADEX SODIUM
Active substance: sugammadex
SOLUTION · SUGAMMADEX SODIUM 500 mg/5mL
United StatesActive
Marketing holder: Par Health USA, LLC
Verified 2026-10-09 · openFDA NDC
Analogues in other countries- Source: openFDA NDC
- Countries with the substance registered: 2
Composition
- SUGAMMADEX SODIUM · 500 mg/5mL
Analogues by country
Products with the same active substance registered in other countries.
| Country | Products |
|---|---|
| EU 7 |
|
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
Registration
- Registration number
- 42023-935
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- INTRAVENOUS
Sources
- product · openFDA NDC · 42023-935 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 42023-935 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 42023-935 · Verified 2026-10-09 · open in source