Wydase® (hyaluronidase)

BL 006343

Wydase® (hyaluronidase)

BL 006343

U.S. License Holder:

Baxter Healthcare

Date of License:

March-22-1950

Last Update:

Feb-15-2025

approved_indications FDA-Approved Indications

WYDASE (hyaluronidase) FDA labeling information is not available.

approved_indications aBLA / 505(b)(2) Activity

aBLA / 505(b)(2) Approved by FDA

Vitrase®: Bausch and Lomb (May-2004) Amphadase®: Amphastar Pharmaceuticals (October-2004) Hydase®: Akorn, Inc. (October-2005) Hylenex®: Halozyme Therapeutics, Inc. (December-2005)

Methodology

Information contained in the Venable BiologicsHQ database relates to FDA-approved drug products listed in the CDER Purple Book or on the FDA website (www.fda.gov). Information relating to FDA licensed products, FDA-approved indications, and aBLA and 505(b)(2) applications is obtained from public sources including the U.S. FDA website (www.fda.gov). Information relating to litigations is given only for cases active from January 31, 2010 onward. Information relating to foreign biosimilar / biologics follow-on products approved in Australia, Canada, the E.U., Japan and South Korea is from public sources. Statistics graphics are compiled from information contained in the Venable BiologicsHQ database.

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