Approvals/TGA/ACICLOVIR VIATRIS aciclovir (as sodium) 250 mg powder for injection vial

Approved

STANDARD

ACICLOVIR VIATRIS aciclovir (as sodium) 250 mg powder for injection vial

Alphapharm Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 42c80db3fe826f08
Product Name: ACICLOVIR VIATRIS aciclovir (as sodium) 250 mg powder for injection vial
Artg Id: 233649
Artg Name: ACICLOVIR VIATRIS aciclovir (as sodium) 250 mg powder for injection vial
Sponsor: Alphapharm Pty Ltd
Company Detail Path: /organization/alphapharm-pty-ltd
Artg Date: 2021-05-28
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-2023-CMI-01235-1
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2021-PI-01764-1

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

42c80db3fe826f08

Type

Standard