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GAVILYTE-N

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

POWDER, FOR SOLUTION · POLYETHYLENE GLYCOL 3350 420 g/438.4g, SODIUM CHLORIDE 11.2 g/438.4g, SODIUM BICARBONATE 5.72 g/438.4g, POTASSIUM CHLORIDE 1.48 g/438.4g

United StatesActive

Marketing holder: Lupin Pharmaceuticals,Inc.

Verified 2026-10-09 · openFDA NDC

Composition
Registration
Registration number
43386-050
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 43386-050 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 43386-050 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 43386-050 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 43386-050 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 43386-050 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 43386-050 · Verified 2026-10-09 · open in source