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Trichophyton rubrum

NDC 49643-175 · NON-STANDARDIZED ALLERGENIC · LIQUID

Labeler / ManufacturerAllermed Laboratories, Inc.
Marketing categoryBiologic License Application · App BLA102211
Dosage form / routeLIQUID · PERCUTANEOUS SUBCUTANEOUS
Active ingredientsTRICHOPHYTON RUBRUM (.1 g/mL)
Marketing started19740312
Package count4

External sources

Source: openFDA. Public-domain (CC0).