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RABBIT

NDC 0268-0651 · NON-STANDARDIZED ALLERGENIC · INJECTION, SOLUTION

Labeler / ManufacturerALK-Abello, Inc.
Marketing categoryBiologic License Application · App BLA103753
Dosage form / routeINJECTION, SOLUTION · SUBCUTANEOUS
Active ingredientsRABBIT (.05 g/mL)
Marketing started19650101
Package count1

External sources

Source: openFDA. Public-domain (CC0).