Fusarium moniliforme
Solution · Intradermal, Percutaneous, Subcutaneous
No FDA structured label text is available for Fusarium moniliforme. The NDC listings below come from the FDA National Drug Code directory.
Active ingredients
- Gibberella Fujikuroi in 6 products
Fusarium moniliforme NDC products (6)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 22840-1670 | Gibberella Fujikuroi .1 g/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-1671 | Gibberella Fujikuroi 20000 [PNU]/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-1672 | Gibberella Fujikuroi .05 g/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-1673 | Gibberella Fujikuroi 40000 [PNU]/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-1674 | Gibberella Fujikuroi .001 g/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-5618 | Gibberella Fujikuroi .05 g/mL Solution | Greer Laboratories, Inc. | BLA |
Frequently asked questions
Who makes Fusarium moniliforme?
Fusarium moniliforme is listed by 1 labeler in the FDA NDC directory, including Greer Laboratories, Inc..