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NDC 49471-001 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic namebenzylpenicilloyl polylysine
Labeler / ManufacturerALK-ABELLO, INC.
Marketing categoryBiologic License Application · App BLA050114
Dosage form / routeINJECTION · INTRADERMAL SUBCUTANEOUS
Active ingredientsBENZYLPENICILLOYL POLYLYSINE (60 umol/.25mL)
Marketing started19740725
Package count1

External sources

Source: openFDA. Public-domain (CC0).