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Common Mugwort

NDC 22840-1348 · NON-STANDARDIZED ALLERGENIC · SOLUTION

Generic nameArtemisia vulgaris
Labeler / ManufacturerGreer Laboratories, Inc.
Marketing categoryBiologic License Application · App BLA101833
Dosage form / routeSOLUTION · INTRADERMAL PERCUTANEOUS SUBCUTANEOUS
Active ingredientsARTEMISIA VULGARIS POLLEN (.001 g/mL)
Marketing started19810915
Package count1

External sources

Source: openFDA. Public-domain (CC0).