Approvals/TGA/ALIMTA pemetrexed 500mg (as disodium heptahydrate) powder for injection vial

Approved

STANDARD

ALIMTA pemetrexed 500mg (as disodium heptahydrate) powder for injection vial

Eli Lilly Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 12650af7e078348e
Product Name: ALIMTA pemetrexed 500mg (as disodium heptahydrate) powder for injection vial
Artg Id: 96731
Artg Name: ALIMTA pemetrexed (as disodium) 500mg powder for injection vial
Sponsor: Eli Lilly Australia Pty Ltd
Company Detail Path: /organization/eli-lilly-australia-pty-ltd
Artg Date: 2004-06-30
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/465a95600648b019f06c113538c95f83.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/f4786d3d8df0ef71520d8b4dc6f7831b.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 29, 2025

Approval ID

12650af7e078348e

Type

Standard