Fire Ant .05 g/mL
Solenopsis richteri · SOLUTION · Greer Laboratories, Inc.
Fire Ant (Solenopsis richteri) is an over-the-counter injectable solution administered under the skin that contains fire ant extract at a strength of 0.05 g/mL. This product is used for immunotherapy to help desensitize patients to fire ant venom and reduce allergic reactions to fire ant stings.
Key Facts
- Brand Name
- Fire Ant
- Generic Name
- Solenopsis richteri
- NDC Code (Product)
22840-5002- Manufacturer
- Greer Laboratories, Inc.
- Strength
- .05 g/mL
- Dosage Form
- SOLUTION
- Route
- INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
- Marketing Status
- Application #
- BLA101833
- Marketing Start
- 09/15/1981
Recall History
No Recall HistoryFrequently Asked Questions
What is Fire Ant used for?
Fire Ant (Solenopsis richteri) is an over-the-counter injectable solution administered under the skin that contains fire ant extract at a strength of 0.05 g/mL. This product is used for immunotherapy to help desensitize patients to fire ant venom and reduce allergic reactions to fire ant stings.
Is Fire Ant a controlled substance?
Fire Ant is not classified as a controlled substance by the DEA.
What is the generic name for Fire Ant?
The generic name for Fire Ant is Solenopsis richteri. There are no other listed brand versions of Solenopsis richteri.
What is the NDC code for Fire Ant .05 g/mL?
The NDC (National Drug Code) for Fire Ant .05 g/mL is 22840-5002, listed by Greer Laboratories, Inc..
Other Fire Ant Dosages
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)