FDA NDC Directory · JSON-LD · Markdown

Polyethylene Glycol

NDC 68001-505 · HUMAN OTC DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerBluePoint Laboratories
Marketing categoryAbbreviated NDA (generic) · App ANDA091077
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsPOLYETHYLENE GLYCOL 3350 (17 g/17g)
Marketing started20210618
Package count2

External sources

Source: openFDA. Public-domain (CC0).