Data / Drug companies / Non-Standardized Insect Allergenic Extract
Non-Standardized Insect Allergenic Extract drugs: 15 drugs from 23 companies in the FDA NDC directory
Non-Standardized Insect Allergenic Extract is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 91 products in this class from 23 companies, covering 15 drugs by generic name. The main marketing category is unapproved homeopathic products, and the newest product started marketing on April 10, 2026.
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- 23Companies
- 91Products
- 15Drugs by generic name
Drugs in the Non-Standardized Insect Allergenic Extract class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Blatta orientalis | 13 | 2 |
| Blattella germanica | 4 | 2 |
| Periplaneta americana | 4 | 2 |
| Insects whole body cockroach mix | 6 | 1 |
| Musca domestica | 5 | 1 |
| Aedes taeniorhynchus | 4 | 1 |
| Bombyx mori | 3 | 1 |
| Periplaneta americana and blattella germanica | 3 | 1 |
| American cockroach | 2 | 1 |
| Blatella germanica and periplaneta americana | 2 | 1 |
| Ctenocephalides felis | 2 | 1 |
| German cockroach | 2 | 1 |
| Blattella germanica and periplaneta americana | 1 | 1 |
| Insects whole body cockroach, american periplaneta americana | 1 | 1 |
| Insects whole body cockroach, german blatella germanica | 1 | 1 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Greer Laboratories, Inc. | 23 | solution | Biologics (BLA) | September 15, 1981 |
| Deseret Biologicals, Inc. | 12 | liquid | Unapproved homeopathic products | April 10, 2026 |
| Jubilant HollisterStier LLC | 8 | injection, solution | Biologics (BLA) | April 19, 1941 |
| ALK-Abello, Inc. | 7 | injection, solution | Biologics (BLA) | February 23, 1998 |
| Hahnemann Laboratories, Inc. | 7 | pellet | Unapproved homeopathic products | May 3, 2022 |
| Boiron | 6 | pellet | Unapproved homeopathic products | January 1, 2024 |
| Professional Complementary Health Formulas | 5 | liquid | Unapproved homeopathic products | August 15, 1984 |
| Newton Laboratories, Inc. | 3 | liquid; pellet | Unapproved homeopathic products | September 2, 2019 |
| Allermed Laboratories, Inc. | 2 | injection | Biologics (BLA) | March 12, 1974 |
| Apex Energetics Inc. | 2 | solution/ drops | Unapproved homeopathic products | November 1, 1994 |
| Dna Labs, Inc. | 2 | solution | Unapproved homeopathic products | January 1, 1990 |
| Energique, Inc. | 2 | liquid | Unapproved homeopathic products | May 27, 2021 |
| Natural Creations, Inc | 2 | liquid | Unapproved homeopathic products | July 12, 2012 |
| Be Well Medical DBA Richard Clement Nutrition Y Be Well Homeopathics | 1 | liquid | Unapproved homeopathic products | November 25, 2014 |
| BioActive Nutritional, Inc. | 1 | liquid | Unapproved homeopathic products | April 6, 2023 |
| Guna Spa | 1 | solution/ drops | Unapproved homeopathic products | May 27, 2010 |
| Homeocare Laboratories | 1 | pellet | Unapproved homeopathic products | April 1, 2021 |
| Liddell Laboratories, Inc. | 1 | spray | Unapproved homeopathic products | October 5, 2021 |
| Meditrend, Inc. DBA Progena Professional Formulations | 1 | liquid | Unapproved homeopathic products | June 19, 2024 |
| NaturalCare | 1 | tablet | Unapproved homeopathic products | February 3, 2026 |
| Nutritional Specialties, Inc. | 1 | spray | Unapproved homeopathic products | October 13, 2023 |
| Ohm Pharma Inc. | 1 | liquid | Unapproved homeopathic products | June 2, 2017 |
| Seroyal USA | 1 | liquid | Unapproved homeopathic products | December 16, 2015 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Liquid | 28 | 30.8% |
| Solution | 25 | 27.5% |
| Injection, solution | 15 | 16.5% |
| Pellet | 15 | 16.5% |
| Solution/ drops | 3 | 3.3% |
| Injection | 2 | 2.2% |
| Spray | 2 | 2.2% |
| Tablet | 1 | 1.1% |
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.