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TRILYTE

NDC 84386-013 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION

Generic namepolyethylene glyocol 3350, sodium chloride, sodium bicarbonate and potassium chloride
Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA076491
Dosage form / routePOWDER, FOR SOLUTION · ORAL
Active ingredientsPOLYETHYLENE GLYCOL 3350 (420 g/4L)
POTASSIUM CHLORIDE (1.48 g/4L)
SODIUM BICARBONATE (5.72 g/4L)
SODIUM CHLORIDE (11.2 g/4L)
Marketing started20260414
Package count1

External sources

Source: openFDA. Public-domain (CC0).