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Data / Drug companies / Folate Analog Metabolic Inhibitor

Folate Analog Metabolic Inhibitor drugs: 6 drugs from 56 companies in the FDA NDC directory

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Folate Analog Metabolic Inhibitor is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 152 products in this class from 56 companies, covering 6 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on October 29, 2026.

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  • 56Companies
  • 152Products
  • 6Drugs by generic name

Drugs in the Folate Analog Metabolic Inhibitor class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Methotrexate7231
Pemetrexed disodium4414
Pemetrexed229
Methotrexate sodium65
Pralatrexate63
Pemetrexed dipotassium21

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Medexus Pharma, Inc.9injection, solutionNew drug applications (NDA)July 10, 2014
BluePoint Laboratories8injection, powder, lyophilized, for solutionGeneric drugs (ANDA)February 28, 2023
Meitheal Pharmaceuticals Inc.8injection, powder, lyophilized, for solutionGeneric drugs (ANDA)December 13, 2022
Antares Pharma, Inc.7injection, solutionNew drug applications (NDA)October 11, 2013
Eugia US LLC7injection, solution; injection, powder, lyophilized, for solutionGeneric drugs (ANDA)September 11, 2024
Fresenius Kabi USA, LLC6injection, powder, lyophilized, for solution; injection, solutionGeneric drugs (ANDA)May 25, 2022
Hikma Pharmaceuticals USA Inc.6solution; injection, powder, lyophilized, for solutionGeneric drugs (ANDA)January 5, 2018
Hospira, Inc.6injection, solutionNew drug applications (NDA)November 4, 2024
Hospira, Inc.6injection, solution, concentrateNew drug applications (NDA)February 1, 2023
Accord Healthcare Inc.5injection, powder, lyophilized, for solution; injectionGeneric drugs (ANDA)May 25, 2022
Dr. Reddy's Laboratories Inc.5injection, powder, lyophilized, for solution; injectionGeneric drugs (ANDA)March 4, 2026
Avyxa Pharma, LLC4injection, powder, lyophilized, for solutionNew drug applications (NDA)January 1, 2025
Bryant Ranch Prepack4tabletGeneric drugs (ANDA)August 24, 2020
Teva Women's Health LLC4tablet, film coatedGeneric drugs (ANDA)May 3, 2001
Alembic Pharmaceuticals Inc.3injection, solution; tabletGeneric drugs (ANDA)April 15, 2026
Alembic Pharmaceuticals Limited3injection, solution; tabletGeneric drugs (ANDA)April 15, 2026
Amneal Pharmaceuticals LLC3injectionNew drug applications (NDA)June 6, 2023
Sandoz Inc3injection, solutionNew drug applications (NDA)June 8, 2022
Shilpa Medicare Limited3injectionNew drug applications (NDA)January 1, 2024
Teva Parenteral Medicines, Inc.3injection, solutionGeneric drugs (ANDA)August 1, 2012
Teva Pharmaceuticals, Inc.3solution, concentrateNew drug applications (NDA)June 1, 2022
Acrotech Biopharma Inc2injectionNew drug applications (NDA)September 24, 2009
Bryant Ranch Prepack2tabletGeneric drugs (ANDA)June 4, 2024
Camber Pharmaceuticals, Inc.2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)June 14, 2024
Eli Lilly and Company2injection, powder, lyophilized, for solutionNew drug applications (NDA)September 7, 2007
Fresenius Kabi USA, LLC2injectionAuthorized generics (NDA)November 15, 2022
NorthStar RxLLC2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)October 1, 2024
NuCare Pharmaceuticals,Inc.2tabletGeneric drugs (ANDA)August 24, 2020
Qilu Pharmaceutical Co., Ltd.2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)May 25, 2022
Sagent Pharmaceuticals2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)December 15, 2024
Somerset Therapeutics, LLC2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)April 15, 2025
Waverley Pharma Inc2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)June 4, 2018
A-S Medication Solutions1tabletGeneric drugs (ANDA)November 1, 1990
Acacia Pharma, Ltd.1injectionNew drug applications (NDA)June 22, 2026
American Health Packaging1tabletGeneric drugs (ANDA)October 29, 2026
Aurobindo Pharma Limited1tabletGeneric drugs (ANDA)January 30, 2020
AvKARE1tabletGeneric drugs (ANDA)November 20, 2014
AvPAK1tabletGeneric drugs (ANDA)January 29, 2026
Azurity Pharmaceuticals, Inc.1solutionNew drug applications (NDA)May 1, 2017
Chartwell RX, LLC1tabletGeneric drugs (ANDA)January 30, 2020
Coupler LLC1tabletGeneric drugs (ANDA)February 27, 2025
Eagle Pharmaceuticals, Inc.1injectionNew drug applications (NDA)February 1, 2022
Elite Laboratories, Inc.1tabletGeneric drugs (ANDA)May 16, 2024
Golden State Medical Supply, Inc.1tabletGeneric drugs (ANDA)May 15, 1992
Hikma Pharmaceuticals USA Inc.1tabletGeneric drugs (ANDA)August 1, 1994
Major Pharmaceuticals1tabletGeneric drugs (ANDA)February 9, 2017
Mylan Institutional Inc.1tabletGeneric drugs (ANDA)July 13, 1995
Mylan Pharmaceuticals Inc.1tabletGeneric drugs (ANDA)May 18, 1992
Proficient Rx LP1tabletGeneric drugs (ANDA)August 24, 2020
Safecor Health, LLC1tabletGeneric drugs (ANDA)January 19, 2026
Shorla Oncology Inc.1solutionNew drug applications (NDA)December 15, 2023
Solco Healthcare US, LLC1injection, powder, for solutionGeneric drugs (ANDA)July 1, 2024
Sun Pharmaceutical Industries, Inc.1tabletGeneric drugs (ANDA)November 10, 2017
Teva Pharmaceuticals USA, Inc.1tabletGeneric drugs (ANDA)November 1, 1990
Zydus Lifesciences Limited1tabletGeneric drugs (ANDA)February 9, 2017
Zydus Pharmaceuticals USA Inc.1tabletGeneric drugs (ANDA)February 9, 2017

Dosage forms

Dosage formProductsShare
Injection, powder, lyophilized, for solution5032.9%
Injection, solution3724.3%
Tablet3019.7%
Injection159.9%
Solution63.9%
Injection, solution, concentrate63.9%
Tablet, film coated42.6%
Solution, concentrate32%
Injection, powder, for solution10.7%

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.