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Data / Drug companies / Iodine

Iodine: 5 companies and 11 products in the FDA NDC directory

Iodine is listed in the FDA National Drug Code Directory by 5 companies, with 11 products in commercial distribution. 0 of the products (0.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are pellet; liquid; tincture, and the newest product started marketing on March 9, 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
5
Products
11
Generic (ANDA) products
0 (0.0%)
Application numbers
1
Routes
Oral, Topical
Brand names
Iodium
openFDA record search
api.fda.gov

Companies that list iodine

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Boiron7pelletUnapproved homeopathic productsMarch 3, 1983
Evi Labs1tinctureOver the counter monograph drugsMarch 9, 2026
Nice-Pak Products, LLC1liquidOver the counter monograph drugsAugust 7, 2017
United Natural Foods, Inc. DBA Unfi1liquidOver the counter monograph drugsFebruary 4, 2005
Walgreen Company1liquidOver the counter monograph drugsMarch 11, 2011

Dosage forms

Dosage formProductsShare
Pellet763.6%
Liquid327.3%
Tincture19.1%

Marketing categories

Marketing categoryProductsShare
Unapproved homeopathic products763.6%
Over the counter monograph drugs436.4%

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.