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Data / Drug companies / Vecuronium bromide

Vecuronium bromide: 10 companies and 20 products in the FDA NDC directory

Vecuronium bromide is listed in the FDA National Drug Code Directory by 10 companies, with 20 products in commercial distribution. 20 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are injection, powder, lyophilized, for solution; injection, powder, for solution; injection, and the newest product started marketing on December 5, 2025.

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.

Companies listing it
10
Products
20
Generic (ANDA) products
20 (100.0%)
Application numbers
6
Routes
Intravenous
openFDA record search
api.fda.gov

Companies that list vecuronium bromide

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Eugia US LLC4injection, powder, lyophilized, for solutionGeneric drugs (ANDA)December 20, 2018
Gland Pharma Limited2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)June 30, 2016
HF Acquisition Co LLC, DBA HealthFirst2injection, powder, lyophilized, for solution; injection, powder, for solutionGeneric drugs (ANDA)July 31, 2022
Hikma Pharmaceuticals USA Inc.2injection, powder, for solutionGeneric drugs (ANDA)August 1, 2019
Meitheal Pharmaceuticals Inc.2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)July 1, 2025
Mullan Pharmaceutical Inc.2injectionGeneric drugs (ANDA)December 5, 2025
Mylan Institutional LLC2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)August 19, 2015
Sagent Pharmaceuticals2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)July 1, 2024
Phlow Corporation1injection, powder, for solutionGeneric drugs (ANDA)August 1, 2019
Sun Pharmaceutical Industries, Inc.1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)December 15, 2014

Dosage forms

Dosage formProductsShare
Injection, powder, lyophilized, for solution1470%
Injection, powder, for solution420%
Injection210%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)20100%

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.