Skip to the page

Data / Drug companies / Atazanavir

Atazanavir: 4 companies and 13 products in the FDA NDC directory

Atazanavir is listed in the FDA National Drug Code Directory by 4 companies, with 13 products in commercial distribution. 10 of the products (76.9%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are capsule; capsule, gelatin coated; powder, and the newest product started marketing on February 7, 2022.

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
4
Products
13
Generic (ANDA) products
10 (76.9%)
Application numbers
5
Routes
Oral
Brand names
Reyataz
openFDA record search
api.fda.gov

Companies that list atazanavir

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Aurobindo Pharma Limited4capsuleGeneric drugs (ANDA)June 25, 2018
Camber Pharmaceuticals, Inc.3capsuleGeneric drugs (ANDA)February 7, 2022
E.r. Squibb & Sons, L.L.C.3capsule, gelatin coated; powderNew drug applications (NDA)December 19, 2014
Laurus Labs Limited3capsuleGeneric drugs (ANDA)April 30, 2021

Dosage forms

Dosage formProductsShare
Capsule1076.9%
Capsule, gelatin coated215.4%
Powder17.7%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)1076.9%
New drug applications (NDA)323.1%

Pharmacologic classes

ClassProducts
Protease Inhibitor13

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.