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Data / Drug companies / Doxycycline hyclate

Doxycycline hyclate: 61 companies and 186 products in the FDA NDC directory

Doxycycline hyclate is listed in the FDA National Drug Code Directory by 61 companies, with 186 products in commercial distribution. 180 of the products (96.8%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are capsule; tablet, film coated; tablet, and the newest product started marketing on June 22, 2026.

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Companies listing it
61
Products
186
Generic (ANDA) products
180 (96.8%)
Application numbers
37
Routes
Oral, Intravenous
Brand names
Doxycycline, Acticlate Cap, Doryx MPC, Targadox, Doxycyclate Hyclate
openFDA record search
api.fda.gov

Companies that list doxycycline hyclate

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
A-S Medication Solutions11capsule; tablet, film coatedGeneric drugs (ANDA)March 7, 2025
Alembic Pharmaceuticals Inc.11tablet, film coated; tablet, delayed releaseGeneric drugs (ANDA)January 4, 2022
Alembic Pharmaceuticals Limited11tablet, film coated; tablet, delayed releaseGeneric drugs (ANDA)January 4, 2022
Bryant Ranch Prepack11capsule; tabletGeneric drugs (ANDA)January 10, 2022
Remedyrepack Inc.11capsule; tablet, film coatedGeneric drugs (ANDA)May 13, 2026
Chartwell RX, LLC8tablet, film coated; capsuleGeneric drugs (ANDA)July 27, 2021
NuCare Pharmaceuticals,Inc.8capsule; tablet, film coatedGeneric drugs (ANDA)October 9, 2019
PD-Rx Pharmaceuticals, Inc.8tablet, film coated; capsuleGeneric drugs (ANDA)August 21, 2020
Redpharm Drug5tablet; tablet, film coatedGeneric drugs (ANDA)March 7, 2025
Ajanta Pharma USA Inc.4tablet; capsuleGeneric drugs (ANDA)June 1, 2020
Chartwell Governmental & Specialty RX, LLC.4capsule; tablet, film coatedGeneric drugs (ANDA)July 21, 2021
Heritage Pharmaceuticals Inc. D/B/A Avet Pharmaceuticals Inc.4tablet, delayed releaseGeneric drugs (ANDA)March 16, 2018
Proficient Rx LP4tablet; capsuleGeneric drugs (ANDA)January 10, 2022
Proficient Rx LP4capsule; tablet, film coatedGeneric drugs (ANDA)July 10, 1986
Sun Pharmaceutical Industries, Inc.4tablet, film coated; capsuleGeneric drugs (ANDA)May 13, 2005
Actavis Pharma, Inc.3tablet, delayed release; tabletGeneric drugs (ANDA)August 14, 2019
Advanced Rx of Tennessee, LLC3capsuleGeneric drugs (ANDA)March 2, 2023
Asclemed USA, Inc.3capsuleGeneric drugs (ANDA)January 10, 2022
AvPAK3capsule; tablet, film coatedGeneric drugs (ANDA)June 4, 2014
Bryant Ranch Prepack3tablet; capsuleGeneric drugs (ANDA)October 9, 2019
Direct_Rx3capsule; tablet, film coatedGeneric drugs (ANDA)January 3, 2025
Hikma Pharmaceuticals USA Inc.3capsule; tablet, coatedGeneric drugs (ANDA)July 2, 2003
Solco Healthcare US, LLC3tablet, delayed releaseGeneric drugs (ANDA)November 28, 2018
Viona Pharmaceuticals Inc3capsule; tabletGeneric drugs (ANDA)January 10, 2022
Zydus Lifesciences Limited3capsule; tabletGeneric drugs (ANDA)September 12, 2018
Cardinal Health 107, LLC2tablet, coatedGeneric drugs (ANDA)March 22, 2013
Coupler LLC2capsuleGeneric drugs (ANDA)May 26, 2026
Epic Pharma, LLC2tablet; tablet, film coatedGeneric drugs (ANDA)March 7, 2025
Health Department, Oklahoma State2capsule; tablet, film coatedGeneric drugs (ANDA)March 7, 2025
Macleods Pharmaceuticals Limited2capsule; tabletGeneric drugs (ANDA)December 9, 2025
Major Pharmaceuticals2tablet, coated; capsuleGeneric drugs (ANDA)August 5, 2008
Northwind Health Company, LLC2capsule; tablet, coatedGeneric drugs (ANDA)February 27, 2023
PD-Rx Pharmaceuticals, Inc.2capsuleGeneric drugs (ANDA)May 7, 1984
Slate Run Pharmaceuticals, LLC2powder, for solutionGeneric drugs (ANDA)July 22, 2024
Sportpharm LLC2capsuleGeneric drugs (ANDA)January 10, 2022
Strides Pharma Science Limited2tabletGeneric drugs (ANDA)May 14, 2026
Zhejiang Yongtai Pharmaceutical Co., Ltd2capsuleGeneric drugs (ANDA)February 1, 2026
Acella Pharmaceuticals, LLC1tablet, coatedGeneric drugs (ANDA)August 21, 2020
Almirall, LLC1capsuleNew drug applications (NDA)May 31, 2018
American Health Packaging1tablet, coatedGeneric drugs (ANDA)March 8, 2013
American Health Packaging1capsuleGeneric drugs (ANDA)April 17, 2020
Cranbury Pharmaceuticals, LLC1tabletGeneric drugs (ANDA)October 9, 2019
Direct RX1capsuleGeneric drugs (ANDA)January 1, 2014
Golden State Medical Supply, Inc.1tablet, film coatedGeneric drugs (ANDA)September 11, 1984
Hawaii Repack, Inc.1capsuleGeneric drugs (ANDA)September 11, 1984
Hikma Pharmaceuticals1capsuleGeneric drugs (ANDA)September 1, 1990
JG Pharma Inc.1tablet, film coatedGeneric drugs (ANDA)August 1, 2025
Journey Medical Corporation1tabletGeneric drugs (ANDA)August 29, 2016
Larken Laboratories, Inc.1tabletGeneric drugs (ANDA)November 15, 2010
Lupin Pharmaceuticals,Inc.1tabletGeneric drugs (ANDA)September 6, 2017
Mayne Pharma1tablet, delayed releaseAuthorized generics (NDA)February 1, 2016
Mayne Pharma Inc.1tablet, delayed releaseNew drug applications (NDA)January 2, 2023
NCS HealthCare of Ky, LLC DBA Vangard Labs1tabletGeneric drugs (ANDA)March 14, 2019
Novel Laboratories, Inc.1tabletGeneric drugs (ANDA)September 6, 2017
PD-Rx Pharmaceuticals, Inc.1tablet, coatedGeneric drugs (ANDA)July 2, 2003
Puracap Laboratories LLC DBA Blu Pharmaceuticals1tablet, film coatedGeneric drugs (ANDA)March 7, 2025
QPharma, Inc.1tablet, coatedGeneric drugs (ANDA)July 2, 2003
Quality Care Products LLC1capsuleGeneric drugs (ANDA)April 16, 2012
Sonoma Pharmaceuticals, Inc.1tablet, delayed releaseGeneric drugs (ANDA)November 28, 2016
St. Mary's Medical Park Pharmacy1tabletGeneric drugs (ANDA)August 17, 2023
Unit Dose Solutions, Inc.1capsuleGeneric drugs (ANDA)June 22, 2026

Dosage forms

Dosage formProductsShare
Capsule7741.4%
Tablet, film coated4323.1%
Tablet3116.7%
Tablet, delayed release2010.8%
Tablet, coated137%
Powder, for solution21.1%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)18096.8%
Authorized generics (NDA)42.2%
New drug applications (NDA)21.1%

Pharmacologic classes

ClassProducts
Tetracycline-class Drug186

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.