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Standardized Kentucky Blue (June) Grass

NDC 49643-393 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic namePoa pratensis
Labeler / ManufacturerAllermed Laboratories, Inc.
Marketing categoryBiologic License Application · App BLA102215
Dosage form / routeINJECTION · CUTANEOUS INTRADERMAL SUBCUTANEOUS
Active ingredientsPOA PRATENSIS POLLEN (100000 [BAU]/mL)
Marketing started19961202
Package count4

External sources

Source: openFDA. Public-domain (CC0).