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HYALURONIDASE

NDC 51662-1555 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHF Acquisition Co LLC, DBA HealthFirst
Marketing categoryBiologic License Application · App BLA021859
Dosage form / routeINJECTION, SOLUTION · SUBCUTANEOUS
Active ingredientsHYALURONIDASE (HUMAN RECOMBINANT) (150 [USP'U]/mL)
Marketing started20210604
Package count1

External sources

Source: openFDA. Public-domain (CC0).