Assyro AI
FDA Purple Book · Reference family

pertuzumab, trastuzumab, and hyaluronidase-zzxf (Phesgo)

pertuzumab, trastuzumab, and hyaluronidase-zzxf is an FDA-licensed reference biologic from Genentech, Inc.. Reference exclusivity, biosimilar lineage, and published patents from official FDA Purple Book records.

0

Biosimilars

0

Interchangeables

0

Listed patents

2020

Reference approved

Reference product

351(a)BLA 761170

Phesgo pertuzumab, trastuzumab, and hyaluronidase-zzxf

Genentech, Inc.

Approved
Jun 29, 2020
Marketing
Rx
Center
CDER
Patents
None listed

Exclusivity & patent cliffs

Approval, exclusivity, and published-patent expiration dates for pertuzumab, trastuzumab, and hyaluronidase-zzxf, in chronological order.

  1. Reference approval

    Approval date of the reference pertuzumab, trastuzumab, and hyaluronidase-zzxf product.

    6 yr ago

Frequently asked questions

Are there biosimilars approved for pertuzumab, trastuzumab, and hyaluronidase-zzxf (Phesgo)?

No 351(k) biosimilars or interchangeable biosimilars referencing pertuzumab, trastuzumab, and hyaluronidase-zzxf are listed in the FDA Purple Book yet.

Explore the full FDA Purple Book

Search every FDA-licensed biologic, biosimilar, and interchangeable with exclusivity timelines and patent records.

Open the Purple Book tool