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CENTER-AL - ULMUS AMERICANA POLLEN

NDC 0268-0069 · NON-STANDARDIZED ALLERGENIC · INJECTION, SUSPENSION

Generic nameULMUS AMERICANA POLLEN
Labeler / ManufacturerALK-Abello, Inc.
Marketing categoryBiologic License Application · App BLA103753
Dosage form / routeINJECTION, SUSPENSION · SUBCUTANEOUS
Active ingredientsULMUS AMERICANA POLLEN (10000 [PNU]/mL)
Marketing started19750115
Package count1

External sources

Source: openFDA. Public-domain (CC0).