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Hyalase (hyaluronidase)Hyalase 1500IU powder for injection ampoule

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Hyalase (hyaluronidase) is a Other product (Drug), registered by Sanofi-Aventis Australia Pty Ltd. Linked registrations: UK PL 29831/0113, Australia 27749. Data as of 2026-11-09.

  • Regulatory classOther · Drug
  • HolderSanofi-Aventis Australia Pty Ltd
  • JurisdictionsUK · AU
  • Updated2026-11-09 · v1

Registration and basics are public; findings and prices need an account

Registration and basics

Hyalase (hyaluronidase)

Product
Regulatory class
Drug
Category
Other
UK · MHRA marketing authorisation
PL 29831/0113
Australia · TGA ARTG medicine
27749 (AUST R registered medicine)
Name on registration
HYALURONIDASE 1500 I.U. POWDER FOR SOLUTION FOR INJECTION/INFUSION
Registrant
Wockhardt UK Ltd
First authorisation
Not obtained from an official source
Models and sizes
Powder for solution for injection / infusion. A white, sterile freeze-dried powder for solution for injection or infusion.
Checked against official page
Not yet checked field by field against the live official page

Public: fields from the registration record.Registrant and dates are from PL 29831/0113; 2 registrations linked.

Label facts by jurisdiction

What each jurisdiction's label says for the same attribute; gaps are marked Not reported, irrelevant ones N/A

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Registration timeline

  1. AU

    27749 ARTG start date

First approval, this certificate's issue date (updated after renewals or changes), changes and expiry are listed separately; a missing first approval means it was not obtained from an official source. Up to 6 recent changes per registration; click the number for the full record. Dates on non-Chinese registrations keep the source's wording: UK devices show the registration date (MHRA does not approve them), Australia the ARTG start date, FDA devices the decision date.

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    Sources

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