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Standardized Mite Dermatophagoides pteronyssinus

NDC 22840-0035 · HUMAN PRESCRIPTION DRUG · CONCENTRATE

Generic nameDermatophagoides pteronyssinus
Labeler / ManufacturerGreer Laboratories, Inc.
Marketing categoryBiologic License Application · App BLA101835
Dosage form / routeCONCENTRATE · INTRADERMAL PERCUTANEOUS SUBCUTANEOUS
Active ingredientsDERMATOPHAGOIDES PTERONYSSINUS (5000 [AU]/mL)
Marketing started19890627
Package count2

External sources

Source: openFDA. Public-domain (CC0).