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Data / Drug companies / Etravirine

Etravirine: 7 companies and 16 products in the FDA NDC directory

Etravirine is listed in the FDA National Drug Code Directory by 7 companies, with 16 products in commercial distribution. 11 of the products (68.8%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, and the newest product started marketing on January 1, 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
7
Products
16
Generic (ANDA) products
11 (68.8%)
Application numbers
4
Routes
Oral
Brand names
Intelence
openFDA record search
api.fda.gov

Companies that list etravirine

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Amneal Pharmaceuticals NY LLC3tabletGeneric drugs (ANDA)June 14, 2021
Janssen Products, LP3tabletNew drug applications (NDA)March 26, 2012
AvKARE2tabletGeneric drugs (ANDA)October 4, 2022
Bionpharma Inc.2tabletGeneric drugs (ANDA)January 1, 2026
Carnegie Pharmaceuticals LLC2tabletGeneric drugs (ANDA)June 7, 2022
Leading Pharma, LLC2tabletGeneric drugs (ANDA)June 5, 2022
Patriot Pharmaceuticals2tabletNew drug applications (NDA)April 1, 2025

Dosage forms

Dosage formProductsShare
Tablet16100%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)1168.8%
New drug applications (NDA)531.2%

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.