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Monilia

NDC 49643-113 · NON-STANDARDIZED ALLERGENIC · INJECTION

Generic nameMonilia sitophila
Labeler / ManufacturerAllermed Laboratories, Inc.
Marketing categoryBiologic License Application · App BLA102211
Dosage form / routeINJECTION · CUTANEOUS INTRADERMAL SUBCUTANEOUS
Active ingredientsCHRYSONILIA SITOPHILA (.1 g/mL)
Marketing started19740312
Package count4

External sources

Source: openFDA. Public-domain (CC0).