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TRILYTE

Active substance: POLYETHYLENE GLYCOL 3350, SODIUM BICARBONATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE

POWDER, FOR SOLUTION · POLYETHYLENE GLYCOL 3350 420 g/4L, SODIUM BICARBONATE 5.72 g/4L, SODIUM CHLORIDE 11.2 g/4L, POTASSIUM CHLORIDE 1.48 g/4L

United StatesActive

Marketing holder: Aurobindo Pharma Limited

Verified 2026-10-09 · openFDA NDC

Composition
Registration
Registration number
84386-013
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 84386-013 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 84386-013 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 84386-013 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 84386-013 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 84386-013 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 84386-013 · Verified 2026-10-09 · open in source