Approvals/TGA/VARIVAX REFRIGERATED varicella virus vaccine live powder for injection vial with prefilled diluent syringe

Approved

STANDARD

VARIVAX REFRIGERATED varicella virus vaccine live powder for injection vial with prefilled diluent syringe

Merck Sharp & Dohme (Australia) Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 129cc4367e687d07
Product Name: VARIVAX REFRIGERATED varicella virus vaccine live powder for injection vial with prefilled diluent syringe
Artg Id: 115008
Artg Name: VARIVAX REFRIGERATED varicella virus vaccine live powder for injection vial with prefilled diluent syringe
Sponsor: Merck Sharp & Dohme (Australia) Pty Ltd
Company Detail Path: /organization/merck-sharp-and-dohme-australia-pty-ltd
Artg Date: 2005-03-16
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/30ef55bd258ce4f6e3a0ad9ec5f768db.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/d20e6702f750d7f7bc0609f28f0f83a1.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

129cc4367e687d07

Type

Standard