Skip to the page

Data / Drug companies / Photoenhancer

Photoenhancer drugs: 1 drug from 4 companies in the FDA NDC directory

Photoenhancer is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 6 products in this class from 4 companies, covering 1 drug by generic name. The main marketing category is other unapproved drugs, and the newest product started marketing on May 16, 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.

  • 4Companies
  • 6Products
  • 1Drugs by generic name

Drugs in the Photoenhancer class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Verteporfin for injection22

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Method Pharmaceuticals, LLC3liquidOther unapproved drugsFebruary 24, 2017
Bausch & Lomb Incorporated1injection, powder, lyophilized, for solutionNew drug applications (NDA)April 12, 2000
Bausch Health US LLC1injection, powder, lyophilized, for solutionNew drug applications (NDA)April 12, 2000
V2 Pharma, LLC1capsuleOther unapproved drugsMay 16, 2025

Dosage forms

Dosage formProductsShare
Liquid350%
Injection, powder, lyophilized, for solution233.3%
Capsule116.7%

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.