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Data / Drug companies / Gilead Sciences, Inc.

Gilead Sciences, Inc.: 50 products in the FDA NDC directory, labeler code 61958

Gilead Sciences, Inc. (labeler code 61958) lists 50 products in the FDA National Drug Code Directory, covering 19 finished drugs by generic name. By type: 50 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on October 31, 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.

Labeler code
61958
Products in commercial distribution
50
Packages
65
Finished drugs by generic name
19
Prescription products
50
Over the counter products
0
Flagged as original packager
42 of 42 products that carry the flag
Started marketing in the last 12 months
3
Products with a marketing end date set
5
Earliest marketing start
October 26, 2001
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
New drug applications (NDA)4998%
Biologics (BLA)12%

Products by type

TypeProductsShare
Prescription drugs50100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

DrugProductsCompanies listing it
Tenofovir disoproxil fumarate516
Lenacapavir sodium51
Emtricitabine and tenofovir disoproxil fumarate428
Sofosbuvir41
Ledipasvir and sofosbuvir42
Velpatasvir and sofosbuvir42
Ambrisentan213
Emtricitabine and tenofovir alafenamide21
Emtricitabine23
Idelalisib21
Cobicistat11
Seladelpar lysine11
Sofosbuvir, velpatasvir, and voxilaprevir11
Bictegravir/lenacapavir11
Tenofovir alafenamide11
Bictegravir/lenacapavir, lenacapavir sodium11
Aztreonam15
Bulevirtide11
Remdesivir11

Dosage forms

Dosage formProductsShare
Tablet, film coated2142%
Tablet816%
Pellet612%
Kit510%
Tablet, coated48%
Capsule24%
Injection, powder, lyophilized, for solution24%
Solution12%
Powder12%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Bixlenvo Sunlenca Starter Pack61958-3701KitNew drug applications (NDA)October 31, 2026
Bixlenvo61958-3601Tablet, film coatedNew drug applications (NDA)August 27, 2026
Hepcludex61958-3104Injection, powder, lyophilized, for solutionBiologics (BLA)May 22, 2026
Yeztugo61958-3402KitNew drug applications (NDA)June 18, 2025
Yeztugo61958-3401Tablet, film coatedNew drug applications (NDA)June 18, 2025
Sunlenca61958-3005KitNew drug applications (NDA)March 18, 2025
Biktarvy61958-2506TabletNew drug applications (NDA)October 8, 2024
Livdelzi61958-3301CapsuleNew drug applications (NDA)August 14, 2024
Sunlenca61958-3002KitNew drug applications (NDA)December 22, 2022
Sunlenca61958-3001Tablet, film coatedNew drug applications (NDA)December 22, 2022
Descovy61958-2005TabletNew drug applications (NDA)January 7, 2022
Biktarvy61958-2505TabletNew drug applications (NDA)October 7, 2021
Epclusa61958-2205PelletNew drug applications (NDA)June 10, 2021
Epclusa61958-2204PelletNew drug applications (NDA)June 10, 2021
Veklury61958-2901Injection, powder, lyophilized, for solutionNew drug applications (NDA)November 1, 2020
Epclusa61958-2203Tablet, film coatedNew drug applications (NDA)March 19, 2020
Harvoni61958-1805PelletNew drug applications (NDA)August 28, 2019
Harvoni61958-1804PelletNew drug applications (NDA)August 28, 2019
Harvoni61958-1803Tablet, film coatedNew drug applications (NDA)August 28, 2019
Sovaldi61958-1505PelletNew drug applications (NDA)August 28, 2019
Sovaldi61958-1504PelletNew drug applications (NDA)August 28, 2019
Sovaldi61958-1503Tablet, film coatedNew drug applications (NDA)August 28, 2019
Biktarvy61958-2501TabletNew drug applications (NDA)February 7, 2018
Vosevi61958-2401Tablet, film coatedNew drug applications (NDA)July 18, 2017
Vemlidy61958-2301TabletNew drug applications (NDA)November 10, 2016

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.