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ULMUS AMERICANA POLLEN

NDC 0268-6623 · NON-STANDARDIZED ALLERGENIC · INJECTION, SOLUTION

Generic nameAmerican Elm
Labeler / ManufacturerALK-Abello, Inc.
Marketing categoryBiologic License Application · App BLA103753
Dosage form / routeINJECTION, SOLUTION · PERCUTANEOUS
Active ingredientsULMUS AMERICANA POLLEN (.05 g/mL)
Marketing started19650101
Package count1

External sources

Source: openFDA. Public-domain (CC0).