Skip to the page

Data / Drug companies / Vitamin K

Vitamin K drugs: 3 drugs from 33 companies in the FDA NDC directory

Vitamin K is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 44 products in this class from 33 companies, covering 3 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on October 28, 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.

  • 33Companies
  • 44Products
  • 3Drugs by generic name

Drugs in the Vitamin K class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Phytonadione3731
Vitamin k1 - phytonadione11
Vitamin k1, phytonadione11

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Cipla USA Inc.4injection, emulsion; tabletGeneric drugs (ANDA)January 15, 2025
Fresenius Kabi USA, LLC4emulsion; injection, emulsionUnapproved drugs for a shortageMay 10, 2025
HF Acquisition Co LLC, DBA HealthFirst3injection, emulsionGeneric drugs (ANDA)November 1, 2021
Dr. Reddy's Laboratories Inc.2injection, emulsionGeneric drugs (ANDA)October 5, 2026
Henry Schein, Inc.2injection, emulsionGeneric drugs (ANDA)January 13, 2022
Hospira, Inc.2injection, emulsionGeneric drugs (ANDA)July 27, 2005
Agnitio Inc.1tabletGeneric drugs (ANDA)February 11, 2022
Alembic Pharmaceuticals Inc.1injection, emulsionGeneric drugs (ANDA)September 8, 2025
Alembic Pharmaceuticals Limited1injection, emulsionGeneric drugs (ANDA)September 8, 2025
American Health Packaging1tabletGeneric drugs (ANDA)June 21, 2018
Amneal Pharmaceuticals LLC1injection, emulsionGeneric drugs (ANDA)November 4, 2025
Amneal Pharmaceuticals NY LLC1tabletGeneric drugs (ANDA)May 15, 2018
Amneal Pharmaceuticals Private Limited1injection, emulsionGeneric drugs (ANDA)June 1, 2026
Baxter Healthcare Corporation1injection, emulsionGeneric drugs (ANDA)February 26, 2026
Bottled Science, Inc.1sprayUnapproved homeopathic productsJuly 24, 2019
Caplin Steriles Limited1injection, emulsionGeneric drugs (ANDA)April 26, 2025
Coupler LLC1tabletGeneric drugs (ANDA)September 8, 2025
Exelan Pharmaceuticals Inc.1tabletGeneric drugs (ANDA)December 1, 2023
Gland Pharma Limited1injection, emulsionGeneric drugs (ANDA)December 10, 2024
Glenmark Pharmaceuticals Inc., USA1injection, emulsionGeneric drugs (ANDA)December 10, 2024
International Medication Systems, Limited1injection, emulsionGeneric drugs (ANDA)April 18, 2003
Major Pharmaceuticals1tabletGeneric drugs (ANDA)May 15, 2018
NorthStar Rx LLC1tabletGeneric drugs (ANDA)March 22, 2022
Orbicular Pharmaceutical Technologies Private Limited1injection, emulsionGeneric drugs (ANDA)March 24, 2026
Padagis US LLC1tabletGeneric drugs (ANDA)October 28, 2026
PureTek Corporation1tabletOther unapproved drugsJanuary 26, 2024
Safecor Health, LLC1tabletGeneric drugs (ANDA)September 2, 2026
Sagent Pharmaceuticals1injection, emulsionGeneric drugs (ANDA)February 1, 2026
ScieGen Pharmaceuticals, Inc.1tabletGeneric drugs (ANDA)July 28, 2023
Sun Pharmaceutical Industries, Inc.1injection, emulsionGeneric drugs (ANDA)June 10, 2026
Xiromed, LLC1injection, emulsionGeneric drugs (ANDA)August 28, 2025
Zydus Lifesciences Limited1tabletGeneric drugs (ANDA)February 22, 2019
Zydus Pharmaceuticals USA Inc.1tabletGeneric drugs (ANDA)February 22, 2019

Dosage forms

Dosage formProductsShare
Injection, emulsion2659.1%
Tablet1431.8%
Emulsion36.8%
Spray12.3%

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.