Approvals/TGA/ONDANSETRON-DRLA ondansetron (as hydrochloride dihydrate) 8 mg film-coated tablet blister pack

Approved

STANDARD

ONDANSETRON-DRLA ondansetron (as hydrochloride dihydrate) 8 mg film-coated tablet blister pack

Dr Reddys Laboratories Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 561a8be289054d99
Product Name: ONDANSETRON-DRLA ondansetron (as hydrochloride dihydrate) 8 mg film-coated tablet blister pack
Artg Id: 163429
Artg Name: ONDANSETRON-DRLA ondansetron (as hydrochloride dihydrate) 8 mg film-coated tablet blister pack
Sponsor: Dr Reddys Laboratories Australia Pty Ltd
Company Detail Path: /organization/dr-reddys-laboratories-australia-pty-ltd
Artg Date: 2010-10-28
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/e8de87c1e7c56e8cf92fdea7ebdeb9d7.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/55fc1e647a1d6a89dc43fb608c3462ea.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

561a8be289054d99

Type

Standard