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Data / Drug companies / Sildenafil citrate

Sildenafil citrate: 24 companies and 55 products in the FDA NDC directory

Sildenafil citrate is listed in the FDA National Drug Code Directory by 24 companies, with 55 products in commercial distribution. 34 of the products (61.8%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet; tablet, film coated; film, and the newest product started marketing on June 22, 2026.

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Companies listing it
24
Products
55
Generic (ANDA) products
34 (61.8%)
Application numbers
15
Routes
Oral, Intravenous
Brand names
Sildenafil, Viagra, Revatio, Vybrique
openFDA record search
api.fda.gov

Companies that list sildenafil citrate

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Viatris Specialty LLC6tablet, film coated; injection, solutionNew drug applications (NDA)June 22, 2026
Ani Pharmaceuticals, Inc.4tablet; for suspensionGeneric drugs (ANDA)August 29, 2023
Ibsa Pharma Inc.4filmNew drug applications (NDA)February 15, 2026
Pfizer Laboratories Div Pfizer Inc4tablet, film coatedNew drug applications (NDA)June 3, 2005
Yaral Pharma Inc.4filmNew drug applications (NDA)February 15, 2026
Mylan Pharmaceuticals Inc.3tablet, film coatedAuthorized generics (NDA)December 1, 2017
Nivagen Pharmaceuticals, Inc.3tabletGeneric drugs (ANDA)June 16, 2021
NorthStar RxLLC3tabletGeneric drugs (ANDA)February 24, 2026
PD-Rx Pharmaceuticals, Inc.3tabletGeneric drugs (ANDA)June 16, 2021
Proficient Rx LP3tabletGeneric drugs (ANDA)September 4, 2020
Umedica Laboratories USA Inc.3tablet, film coatedGeneric drugs (ANDA)February 15, 2026
A-S Medication Solutions2tabletGeneric drugs (ANDA)September 4, 2020
Advanced Rx of Tennessee, LLC2tabletGeneric drugs (ANDA)March 20, 2025
Aphena Pharma Solutions - Tennessee, LLC1tabletGeneric drugs (ANDA)February 24, 2026
Ascend Laboratories, LLC1powder, for suspensionGeneric drugs (ANDA)November 29, 2019
Asclemed USA, Inc.1tabletGeneric drugs (ANDA)November 6, 2012
Aurobindo Pharma Limited1powder, for suspensionGeneric drugs (ANDA)December 23, 2022
Eugia US LLC1injection, solutionGeneric drugs (ANDA)April 1, 2015
Novadoz Pharmaceuticals LLC1powder, for suspensionGeneric drugs (ANDA)February 14, 2022
NuCare Pharmaceuticals,Inc.1tablet, film coatedGeneric drugs (ANDA)October 12, 2018
Preferred Pharmaceuticals Inc.1tabletGeneric drugs (ANDA)January 20, 2025
Proficient Rx LP1tabletGeneric drugs (ANDA)June 16, 2021
Zydus Lifesciences Limited1powder, for suspensionGeneric drugs (ANDA)October 27, 2022
Zydus Pharmaceuticals USA Inc.1powder, for suspensionGeneric drugs (ANDA)October 27, 2022

Dosage forms

Dosage formProductsShare
Tablet2341.8%
Tablet, film coated1527.3%
Film814.5%
Powder, for suspension610.9%
Injection, solution23.6%
For suspension11.8%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)3461.8%
New drug applications (NDA)1832.7%
Authorized generics (NDA)35.5%

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.