Approvals/TGA/ZITHROMAX IV azithromycin (as dihydrate) 500mg powder for injection vial

Approved

STANDARD

ZITHROMAX IV azithromycin (as dihydrate) 500mg powder for injection vial

Pfizer Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 9f1edd0460c5e1e7
Product Name: ZITHROMAX IV azithromycin (as dihydrate) 500mg powder for injection vial
Artg Id: 91913
Artg Name: ZITHROMAX IV azithromycin (as dihydrate) 500mg powder for injection vial
Sponsor: Pfizer Australia Pty Ltd
Company Detail Path: /organization/pfizer-australia-pty-ltd
Artg Date: 2002-11-19
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/38814899fb994c6630b8525351cd9328.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/a95e3a9f2927afd94b39e22dcd6553c2.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

9f1edd0460c5e1e7

Type

Standard