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Data / Drug companies / Contrast Agent for Ultrasound Imaging

Contrast Agent for Ultrasound Imaging drugs: 3 drugs from 3 companies in the FDA NDC directory

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

Contrast Agent for Ultrasound Imaging is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 5 products in this class from 3 companies, covering 3 drugs by generic name. The main marketing category is new drug applications (NDA), and the newest product started marketing on April 1, 2021.

The request: Get every company that lists a Contrast Agent for Ultrasound Imaging drug in the FDA NDC directory, with headquarters, website and size. $10 of work on sign-up, no card.

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.

  • 3Companies
  • 5Products
  • 3Drugs by generic name

Drugs in the Contrast Agent for Ultrasound Imaging class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Perflutren21
Sulfur hexafluoride21
Human albumin microspheres and perflutren11

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Bracco Diagnostics Inc2injection, powder, lyophilized, for suspensionNew drug applications (NDA)April 1, 2021
Lantheus Medical Imaging, Inc.2injection, suspensionNew drug applications (NDA)October 1, 2020
GE Healthcare Inc.1injection, solutionNew drug applications (NDA)January 2, 2002

Dosage forms

Dosage formProductsShare
Injection, powder, lyophilized, for suspension240%
Injection, suspension240%
Injection, solution120%

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.