Approvals/TGA/CIPROFLOXACIN SANDOZ ciprofloxacin (as hydrochloride) 500 mg tablet blister pack

Approved

STANDARD

CIPROFLOXACIN SANDOZ ciprofloxacin (as hydrochloride) 500 mg tablet blister pack

Sandoz Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 37a57a1997d0389b
Product Name: CIPROFLOXACIN SANDOZ ciprofloxacin (as hydrochloride) 500 mg tablet blister pack
Artg Id: 81461
Artg Name: CIPROFLOXACIN SANDOZ ciprofloxacin (as hydrochloride) 500 mg tablet blister pack
Sponsor: Sandoz Pty Ltd
Company Detail Path: /organization/sandoz-pty-ltd
Artg Date: 2002-04-26
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2010-CMI-02273-3
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2010-PI-02267-3

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

37a57a1997d0389b

Type

Standard