Spring Birch Pollen
Betula fontinalis · Solution · Intradermal, Subcutaneous, Percutaneous
No FDA structured label text is available for Spring Birch Pollen. The NDC listings below come from the FDA National Drug Code directory.
Active ingredients
- Betula Occidentalis Pollen in 6 products
Spring Birch Pollen NDC products (6)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 49643-441 | Betula Occidentalis Pollen .05 g/mL Injection | Allermed Laboratories, Inc. | BLA |
| 22840-1454 | Betula Occidentalis Pollen .1 g/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-1455 | Betula Occidentalis Pollen 40000 [PNU]/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-1456 | Betula Occidentalis Pollen .001 g/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-4436 | Betula Occidentalis Pollen .05 g/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-5414 | Betula Occidentalis Pollen .05 g/mL Solution | Greer Laboratories, Inc. | BLA |
Frequently asked questions
Who makes Spring Birch Pollen?
Spring Birch Pollen is listed by 2 labelers in the FDA NDC directory, including Allermed Laboratories, Inc., Greer Laboratories, Inc..