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Fosphenytoin

Active substance: fosphenytoin

INJECTION, SOLUTION · FOSPHENYTOIN SODIUM 50 mg/mL

United StatesActive

Marketing holder: Fresenius Kabi USA, LLC

Verified 2026-10-09 · openFDA NDC

Composition
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-4dcb-77ac-871f-27d317a1554f,01a1208c-9877-793e-8559-aff515239db1,01a1208e-af49-7451-9818-e9815134c5ea,01a1208e-bb81-7734-803c-597e9d65b8eb,01a1208e-bf67-7ee8-8b51-d6c787f9942d;count=16 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
63323-403
Registration status
Active
Dispensing
Prescription only
Route
INTRAMUSCULAR, INTRAVENOUS
Sources
  • product · openFDA NDC · 63323-403 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 63323-403 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 63323-403 · Verified 2026-10-09 · open in source