Data / Drug companies / Standardized Pollen Allergenic Extract
Standardized Pollen Allergenic Extract drugs: 35 drugs from 15 companies in the FDA NDC directory
Standardized Pollen Allergenic Extract is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 111 products in this class from 15 companies, covering 35 drugs by generic name. The main marketing category is biologics (BLA), and the newest product started marketing on April 1, 2026.
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- 15Companies
- 111Products
- 35Drugs by generic name
Drugs in the Standardized Pollen Allergenic Extract class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Ambrosia artemisiifolia | 3 | 4 |
| Agrostis alba | 3 | 2 |
| Anthoxanthum odoratum | 3 | 2 |
| Dactylis glomerata | 3 | 2 |
| Festuca elatior | 3 | 2 |
| Lolium perenne | 3 | 2 |
| Phleum pratense | 3 | 2 |
| Poa pratensis | 3 | 2 |
| Cynodon dactylon | 2 | 2 |
| Bermuda grass, standardized | 2 | 1 |
| Giant, short, western ragweed mix | 2 | 1 |
| Kentucky bluegrass june, standardized | 2 | 1 |
| Meadow fescue grass, standardized | 2 | 1 |
| Orchard grass, standardized | 2 | 1 |
| Phleum pratense and dactylis glomerata | 2 | 1 |
| Poa pratensis, dactylis glomerata and phleum pratense | 2 | 1 |
| Ragweed short | 2 | 1 |
| Redtop grass, standardized | 2 | 1 |
| Standardized grass pollen, bluegrass, kentucky june | 2 | 1 |
| Standardized grass pollen, fescue, meadow | 2 | 1 |
| Standardized grass pollen, orchard grass | 2 | 1 |
| Standardized grass pollen, redtop | 2 | 1 |
| Standardized grass pollen, ryegrass | 2 | 1 |
| Standardized grass pollen, sweet vernal grass | 2 | 1 |
| Standardized grass pollen, timothy | 2 | 1 |
| Sweet vernal grass, standardized | 2 | 1 |
| Timothy, standardized | 2 | 1 |
| Ambrosia artemisiifolia and ambrosia trifida | 1 | 1 |
| Lolium perenne pollen | 1 | 1 |
| Mixed ragweed | 1 | 1 |
| Ragweed, mixed ambrosia | 1 | 1 |
| Rye grass, perennial standardized | 1 | 1 |
| Short ragweed, ambrosia artemisiifolia | 1 | 1 |
| Standardized grass pollen, bermuda grass | 1 | 1 |
| Standardized grass pollen, grass mix 4 | 1 | 1 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Greer Laboratories, Inc. | 31 | solution | Biologics (BLA) | September 15, 1981 |
| ALK-Abello, Inc. | 26 | injection, solution; solution | Biologics (BLA) | May 3, 2015 |
| Jubilant HollisterStier LLC | 25 | injection, solution | Biologics (BLA) | January 15, 1998 |
| Allermed Laboratories, Inc. | 9 | injection | Biologics (BLA) | December 2, 1996 |
| BioActive Nutritional, Inc. | 4 | liquid | Unapproved homeopathic products | August 3, 2021 |
| NaturalCare | 3 | liquid; tablet | Unapproved homeopathic products | March 23, 2026 |
| Stallergenes | 3 | tablet, orally disintegrating | Biologics (BLA) | April 30, 2014 |
| Energique, Inc. | 2 | liquid | Unapproved homeopathic products | July 31, 2020 |
| Nutritional Specialties, Inc. | 2 | spray | Unapproved homeopathic products | February 20, 2026 |
| American Standard Nutraceuticals | 1 | liquid | Unapproved homeopathic products | March 26, 2026 |
| Apex Energetics Inc. | 1 | solution/ drops | Unapproved homeopathic products | March 15, 1993 |
| Dna Labs, Inc. | 1 | solution | Unapproved homeopathic products | January 1, 1990 |
| Meditrend, Inc. DBA Progena Professional Formulations | 1 | liquid | Unapproved homeopathic products | April 1, 2026 |
| Natural Creations, Inc | 1 | liquid | Unapproved homeopathic products | May 29, 2007 |
| Ohm Pharma Inc. | 1 | pellet | Unapproved homeopathic products | October 26, 2015 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection, solution | 44 | 39.6% |
| Solution | 39 | 35.1% |
| Liquid | 11 | 9.9% |
| Injection | 9 | 8.1% |
| Tablet, orally disintegrating | 3 | 2.7% |
| Spray | 2 | 1.8% |
| Solution/ drops | 1 | 0.9% |
| Pellet | 1 | 0.9% |
| Tablet | 1 | 0.9% |
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.