American Elm Pollen
Ulmus americana · Solution · Intradermal, Subcutaneous, Percutaneous
No FDA structured label text is available for American Elm Pollen. The NDC listings below come from the FDA National Drug Code directory.
Active ingredients
- Ulmus Americana Pollen in 4 products
American Elm Pollen NDC products (4)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 49643-417 | Ulmus Americana Pollen .05 g/mL Injection | Allermed Laboratories, Inc. | BLA |
| 22840-1492 | Ulmus Americana Pollen .001 g/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-4443 | Ulmus Americana Pollen .1 g/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-5426 | Ulmus Americana Pollen .05 g/mL Solution | Greer Laboratories, Inc. | BLA |
Frequently asked questions
Who makes American Elm Pollen?
American Elm Pollen is listed by 2 labelers in the FDA NDC directory, including Allermed Laboratories, Inc., Greer Laboratories, Inc..