Fusarium solani
Solution · Intradermal, Percutaneous, Subcutaneous
No FDA structured label text is available for Fusarium solani. The NDC listings below come from the FDA National Drug Code directory.
Active ingredients
- Haematonectria Haematococca in 4 products
Fusarium solani NDC products (4)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 22840-1676 | Haematonectria Haematococca .025 g/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-1677 | Haematonectria Haematococca 20000 [PNU]/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-1678 | Haematonectria Haematococca .001 g/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-5619 | Haematonectria Haematococca .025 g/mL Solution | Greer Laboratories, Inc. | BLA |
Frequently asked questions
Who makes Fusarium solani?
Fusarium solani is listed by 1 labeler in the FDA NDC directory, including Greer Laboratories, Inc..