Approvals/TGA/CELESTONE CHRONODOSE betamethasone 5.7 mg/1 mL (as acetate and sodium phosphate) injection ampoule

Approved

STANDARD

CELESTONE CHRONODOSE betamethasone 5.7 mg/1 mL (as acetate and sodium phosphate) injection ampoule

ORGANON PHARMA PTY LTD🇦🇺 Therapeutic Goods Administration

Approval Id: 15e1329d5e8a8a73
Product Name: CELESTONE CHRONODOSE betamethasone 5.7 mg/1 mL (as acetate and sodium phosphate) injection ampoule
Artg Id: 18777
Artg Name: CELESTONE CHRONODOSE betamethasone 5.7mg/1mL (as acetate and sodium phosphate) injection ampoule
Sponsor: ORGANON PHARMA PTY LTD
Company Detail Path: /organization/organon-pharma-pty-ltd
Artg Date: 1991-10-08
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/efa90c0c0440aa678b48fb87bcabb8f5.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/dca0be24c6ef35e8d221d98c557d7333.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

15e1329d5e8a8a73

Type

Standard