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Purple Book
Database of Licensed Biological Products

Product Details for: Phesgo
Product Label Grayed out Product Label links indicate that there is no product label available for the product.

Product NumberDosage FormRoute of AdministrationStrengthProduct PresentationLicense TypeProprietary NameMarketing Status
001Injection Subcutaneous1,200MG, 600MG, 30,000UNITS/15ML (80MG, 40MG, 2,000UNITS/ML)Single-Dose Vial351(a)PhesgoRx
002Injection Subcutaneous600MG, 600MG, 20,000UNITS/10ML (60MG, 60MG, 2,000UNITS/ML)Single-Dose Vial351(a)PhesgoRx

Proper Name
pertuzumab, trastuzumab, and hyaluronidase-zzxf

BLA Number
761170

Applicant
Genentech, Inc.

Original Approval Date
June 29, 2020

Date of First Licensure