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Data / Drug companies / Hydrolytic Lysosomal Glycosaminoglycan-specific Enzyme

Hydrolytic Lysosomal Glycosaminoglycan-specific Enzyme drugs: 4 drugs from 3 companies in the FDA NDC directory

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

Hydrolytic Lysosomal Glycosaminoglycan-specific Enzyme is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 4 products in this class from 3 companies, covering 4 drugs by generic name. The main marketing category is biologics (BLA), and the newest product started marketing on February 14, 2014.

The request: Get every company that lists a Hydrolytic Lysosomal Glycosaminoglycan-specific Enzyme 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
  • 4Products
  • 4Drugs by generic name

Drugs in the Hydrolytic Lysosomal Glycosaminoglycan-specific Enzyme class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Elosulfase alfa11
Galsulfase11
Idursulfase11
Laronidase11

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
BioMarin Pharmaceutical Inc.2injection, solution, concentrate; solutionBiologics (BLA)February 14, 2014
Genzyme Corporation1injection, solution, concentrateBiologics (BLA)April 30, 2003
Takeda Pharmaceuticals America, Inc.1solution, concentrateBiologics (BLA)July 24, 2006

Dosage forms

Dosage formProductsShare
Injection, solution, concentrate250%
Solution, concentrate125%
Solution125%

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.