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Data / Drug companies / Non-Standardized Animal Skin Allergenic Extract

Non-Standardized Animal Skin Allergenic Extract drugs: 24 drugs from 13 companies in the FDA NDC directory

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

Non-Standardized Animal Skin Allergenic Extract is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 92 products in this class from 13 companies, covering 24 drugs by generic name. The main marketing category is biologics (BLA), and the newest product started marketing on September 15, 2025.

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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.

  • 13Companies
  • 92Products
  • 24Drugs by generic name

Drugs in the Non-Standardized Animal Skin Allergenic Extract class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Bos taurus62
Sus scrofa62
Horse epithelia32
Cattle epithelia22
Guinea pig epithelia22
Mouse epithelia22
Equus caballus71
Canis lupus familiaris61
Cavia porcellus61
Oryctolagus cuniculus61
Mus musculus51
Rattus norvegicus51
Meriones unguiculatus41
Mesocricetus auratus41
Capra hircus31
Dog epithelia31
Cattle epithelium11
Dog epithelium11
Goat epithelia11
Guinea pig epithelium11
Hamster epithelia11
Hog epithelia11
Horse epithelium11
Mouse epithelium11

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Greer Laboratories, Inc.58solutionBiologics (BLA)September 15, 1981
ALK-Abello, Inc.13injection, solutionBiologics (BLA)January 1, 1965
Allermed Laboratories, Inc.7injectionBiologics (BLA)March 12, 1974
Apex Energetics Inc.2solution/ dropsUnapproved homeopathic productsJuly 15, 1997
Energique, Inc.2liquidUnapproved homeopathic productsDecember 1, 2020
Meditrend, Inc. DBA Progena Professional Formulations2liquidUnapproved homeopathic productsSeptember 15, 2025
Uriel Pharmacy Inc.2gelUnapproved homeopathic productsSeptember 1, 2009
BioActive Nutritional, Inc.1liquidUnapproved homeopathic productsOctober 6, 2020
Dna Labs, Inc.1solutionUnapproved homeopathic productsJanuary 1, 1990
Guna Spa1pelletUnapproved homeopathic productsMay 23, 2006
Liddell Laboratories, Inc.1sprayUnapproved homeopathic productsJuly 26, 2021
Natural Creations, Inc1liquidUnapproved homeopathic productsMay 29, 2007
Ohm Pharma Inc.1sprayUnapproved homeopathic productsMarch 13, 2013

Dosage forms

Dosage formProductsShare
Solution5964.1%
Injection, solution1314.1%
Injection77.6%
Liquid66.5%
Gel22.2%
Spray22.2%
Solution/ drops22.2%
Pellet11.1%

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.