FDA NDC Directory · JSON-LD · Markdown

Fire Ant

NDC 22840-1005 · NON-STANDARDIZED ALLERGENIC · SOLUTION

Generic nameSolenopsis richteri
Labeler / ManufacturerGreer Laboratories, Inc.
Marketing categoryBiologic License Application · App BLA101833
Dosage form / routeSOLUTION · INTRADERMAL PERCUTANEOUS SUBCUTANEOUS
Active ingredientsSOLENOPSIS RICHTERI (.001 g/mL)
Marketing started19810915
Package count1

External sources

Source: openFDA. Public-domain (CC0).