Data / Drug companies / Allermed Laboratories, Inc.
Allermed Laboratories, Inc.: 199 products in the FDA NDC directory, labeler code 49643
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Allermed Laboratories, Inc. (labeler code 49643) lists 199 products in the FDA National Drug Code Directory, covering 199 finished drugs by generic name. By type: 187 non-standardized allergenic extracts, 12 prescription drugs. Its main marketing category is biologics (BLA). The newest product started marketing on December 2, 1996.
The request: Watch Allermed Laboratories, Inc. (FDA labeler code 49643): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 49643
- Products in commercial distribution
- 199
- Packages
- 794
- Finished drugs by generic name
- 199
- Prescription products
- 12
- Over the counter products
- 0
- Flagged as original packager
- 12 of 12 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- March 12, 1974
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Biologics (BLA) | 199 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Non-standardized allergenic extracts | 187 | 94% |
| Prescription drugs | 12 | 6% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection | 181 | 91% |
| Liquid | 18 | 9% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Standardized Kentucky Blue (June) Grass | 49643-393 | Injection | Biologics (BLA) | December 2, 1996 |
| Standardized Timothy Grass | 49643-386 | Injection | Biologics (BLA) | December 2, 1996 |
| Standardized Perennial Rye Grass | 49643-379 | Injection | Biologics (BLA) | December 2, 1996 |
| Standardized Meadow Fescue Grass | 49643-350 | Injection | Biologics (BLA) | December 2, 1996 |
| Standardized Orchard Grass | 49643-343 | Injection | Biologics (BLA) | December 2, 1996 |
| Standardized Bermuda Grass | 49643-342 | Injection | Biologics (BLA) | December 2, 1996 |
| Standardized Sweet Vernal Grass | 49643-318 | Injection | Biologics (BLA) | December 2, 1996 |
| Standardized Redtop Grass | 49643-309 | Injection | Biologics (BLA) | December 2, 1996 |
| Standardized Cat Hair | 49643-705 | Injection | Biologics (BLA) | August 15, 1992 |
| House Dust Mite, Dermatophagoides pteronyssinus | 49643-704 | Injection | Biologics (BLA) | December 24, 1986 |
| House Dust Mite, Dermatophagoides farinae | 49643-702 | Injection | Biologics (BLA) | December 24, 1986 |
| Short Ragweed | 49643-315 | Injection | Biologics (BLA) | March 22, 1982 |
| Glycerol-Saline Control | 49643-818 | Injection | Biologics (BLA) | March 12, 1974 |
| Trichophyton Mix | 49643-802 | Liquid | Biologics (BLA) | March 12, 1974 |
| Walnut Mix | 49643-544 | Injection | Biologics (BLA) | March 12, 1974 |
| Pine Mix | 49643-524 | Liquid | Biologics (BLA) | March 12, 1974 |
| Maple, California Mix | 49643-520 | Liquid | Biologics (BLA) | March 12, 1974 |
| Alder Mix | 49643-501 | Liquid | Biologics (BLA) | March 12, 1974 |
| Linden Pollen | 49643-460 | Injection | Biologics (BLA) | March 12, 1974 |
| Hard Maple Pollen | 49643-452 | Injection | Biologics (BLA) | March 12, 1974 |
| Black Oak Pollen | 49643-451 | Injection | Biologics (BLA) | March 12, 1974 |
| Red Oak Pollen | 49643-450 | Injection | Biologics (BLA) | March 12, 1974 |
| Yellow Pine Pollen | 49643-449 | Injection | Biologics (BLA) | March 12, 1974 |
| Shortleaf Pine Pollen | 49643-448 | Injection | Biologics (BLA) | March 12, 1974 |
| Red Mulberry Pollen | 49643-447 | Injection | Biologics (BLA) | March 12, 1974 |
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.