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Polyethylene Glycol 3350

NDC 50844-772 · HUMAN OTC DRUG · POWDER, FOR SOLUTION

Labeler / ManufacturerL.N.K. International, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217505
Dosage form / routePOWDER, FOR SOLUTION · ORAL
Active ingredientsPOLYETHYLENE GLYCOL 3350 (17 g/17g)
Marketing started20260910
Package count10

External sources

Source: openFDA. Public-domain (CC0).