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Sucralfate

Active substance: sucralfate

SUSPENSION · SUCRALFATE 1 g/10mL

United StatesActive

Marketing holder: Kesin Pharma Corporation

Verified 2026-10-09 · openFDA NDC

Composition
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-59cd-7928-ac10-cc583531f986,01a1208c-59d9-7150-919c-f4570bb91161,01a1208c-6853-7894-9245-ba3c10680e62,01a1208c-7738-7a3a-a481-72002762a0f7,01a1208c-81f6-702b-a7ce-dfce0b767518;count=69 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
81033-149
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 81033-149 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 81033-149 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 81033-149 · Verified 2026-10-09 · open in source