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Data / Drug companies / Polyethylene glycol

Polyethylene glycol: 2 companies and 2 products in the FDA NDC directory

Polyethylene glycol is listed in the FDA National Drug Code Directory by 2 companies, with 2 products in commercial distribution. 1 of the products (50.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are liquid; powder, for suspension, and the newest product started marketing on May 19, 2026.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Companies listing it
2
Products
2
Generic (ANDA) products
1 (50.0%)
Application numbers
2
Routes
Ophthalmic, Oral
Brand names
Retaine Ultra PF
openFDA record search
api.fda.gov

Companies that list polyethylene glycol

Ranked by number of products. Finished drugs in commercial distribution.

CompanyProductsMain dosage formsMain marketing categoryNewest product started
BluePoint Laboratories1powder, for suspensionGeneric drugs (ANDA)June 18, 2021
OCuSOFT LLC1liquidOver the counter monograph drugsMay 19, 2026

Dosage forms

Dosage formProductsShare
Liquid150%
Powder, for suspension150%

Marketing categories

Marketing categoryProductsShare
Over the counter monograph drugs150%
Generic drugs (ANDA)150%

Pharmacologic classes

ClassProducts
Osmotic Laxative1

Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.