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Data / Drug companies / Triple antibiotic

Triple antibiotic: 5 companies and 7 products in the FDA NDC directory

Triple antibiotic is listed in the FDA National Drug Code Directory by 5 companies, with 7 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 ointment; cream, and the newest product started marketing on September 2, 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
7
Generic (ANDA) products
0 (0.0%)
Application numbers
1
Routes
Topical, Cutaneous
openFDA record search
api.fda.gov

Companies that list triple antibiotic

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Jiangxi Yudexi Pharmaceutical Co., LTD2ointmentOver the counter monograph drugsMarch 21, 2026
Lil' Drug Store Products, Inc.2ointmentOver the counter monograph drugsDecember 28, 2023
Jiangxi He-Oumei Health Industry Co., Ltd.1creamUnapproved homeopathic productsJanuary 24, 2026
Nantong Health & Beyond Hygienic Products Inc.1ointmentOver the counter monograph drugsSeptember 2, 2026
Target Corporation1ointmentOver the counter monograph drugsJanuary 31, 2024

Dosage forms

Dosage formProductsShare
Ointment685.7%
Cream114.3%

Marketing categories

Marketing categoryProductsShare
Over the counter monograph drugs685.7%
Unapproved homeopathic products114.3%

Pharmacologic classes

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.