Approvals/TGA/CEFALEXIN SANDOZ cefalexin (as monohydrate) 250mg/5mL powder for suspension bottle

Approved

STANDARD

CEFALEXIN SANDOZ cefalexin (as monohydrate) 250mg/5mL powder for suspension bottle

Sandoz Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 64c26f8fea6a11d1
Product Name: CEFALEXIN SANDOZ cefalexin (as monohydrate) 250mg/5mL powder for suspension bottle
Artg Id: 78982
Artg Name: CEFALEXIN SANDOZ cefalexin (as monohydrate) 250mg/5mL powder for suspension bottle
Sponsor: Sandoz Pty Ltd
Company Detail Path: /organization/sandoz-pty-ltd
Artg Date: 2002-03-11
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/10f02314c99840b6f4313a2ff13a9b70.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/b3dc18180add552a191f337c2e72e5a2.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

64c26f8fea6a11d1

Type

Standard