Fire Ant
Solenopsis invicta · Solution · Subcutaneous, Intradermal, Percutaneous
No FDA structured label text is available for Fire Ant. The NDC listings below come from the FDA National Drug Code directory.
Active ingredients
- Solenopsis Invicta in 5 products
- Solenopsis Richteri in 2 products
Fire Ant NDC products (7)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 0268-0722 | Solenopsis Invicta .05 g/mL Injection, Solution | ALK-Abello, Inc. | BLA |
| 0268-0724 | Solenopsis Invicta .1 g/mL Injection, Solution | ALK-Abello, Inc. | BLA |
| 22840-1003 | Solenopsis Invicta .001 g/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-1005 | Solenopsis Richteri .001 g/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-1023 | Solenopsis Invicta .1 g/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-5001 | Solenopsis Invicta .05 g/mL Solution | Greer Laboratories, Inc. | BLA |
| 22840-5002 | Solenopsis Richteri .05 g/mL Solution | Greer Laboratories, Inc. | BLA |
Frequently asked questions
Who makes Fire Ant?
Fire Ant is listed by 2 labelers in the FDA NDC directory, including ALK-Abello, Inc., Greer Laboratories, Inc..