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Curvularia

NDC 49643-109 · NON-STANDARDIZED ALLERGENIC · INJECTION

Generic nameCurvularia lunata
Labeler / ManufacturerAllermed Laboratories, Inc.
Marketing categoryBiologic License Application · App BLA102211
Dosage form / routeINJECTION · CUTANEOUS INTRADERMAL SUBCUTANEOUS
Active ingredientsCOCHLIOBOLUS LUNATUS (.1 g/mL)
Marketing started19740312
Package count4

External sources

Source: openFDA. Public-domain (CC0).