Approvals/TGA/ULTIVA Remifentanil (as hydrochloride) 2mg powder for injection vial

Approved

STANDARD

ULTIVA Remifentanil (as hydrochloride) 2mg powder for injection vial

Aspen Pharmacare Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: ad8a14df0b69b753
Product Name: ULTIVA Remifentanil (as hydrochloride) 2mg powder for injection vial
Artg Id: 58689
Artg Name: ULTIVA Remifentanil (as hydrochloride) 2mg powder for injection vial
Sponsor: Aspen Pharmacare Australia Pty Ltd
Company Detail Path: /organization/aspen-pharmacare-australia-pty-ltd
Artg Date: 1998-05-11
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/842daa510874506a5a754ffdff3e8d2d.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

ad8a14df0b69b753

Type

Standard