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Eli Lilly Australia Pty Ltd

Regulatory activities for this sponsor.

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Type

ARTG (73)
Cancellation by sponsor (67)
Australian public assessment report (AusPar) (20)
Prescription medicine registration (20)
Designation or determination (4)
Prescription medicine decision summary (4)
Prescription medicine evaluation (4)

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2026 (4)
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Search

Sponsor content

192 result(s) found, displaying 141 to 150

AXIRON testosterone 2% w/v solution bottle Cancelled under Section 30(1)(c) of the Act

5 March 2019

Cancellation by sponsor

Requested by Eli Lilly Australia Pty Ltd
AusPAR: Ixekizumab

15 January 2019

Australian public assessment report (AusPar)

Australian Public Assessment Report for Ixekizumab
HUMALOG U200 KwikPen insulin lispro (rbe) 200 IU/mL solution for injection multidose syringe (226893)

9 November 2015

ARTG

Australian Register of Therapeutic Goods (ARTG) information for HUMALOG U200 KwikPen insulin lispro (rbe) 200 IU/mL solution for injection multidose syringe.
CYRAMZA ramucirumab 100 mg/10 mL solution for intravenous infusion vial (227351)

23 July 2015

ARTG

Australian Register of Therapeutic Goods (ARTG) information for CYRAMZA ramucirumab 100 mg/10 mL solution for intravenous infusion vial.
CYRAMZA ramucirumab 500 mg/50 mL solution for intravenous infusion vial (227352)

23 July 2015

ARTG

Australian Register of Therapeutic Goods (ARTG) information for CYRAMZA ramucirumab 500 mg/50 mL solution for intravenous infusion vial.
HUMALOG NPL insulin lispro 100U/mL injection multidose cartridge Cancelled under Section 30(1)(c) of the Act

29 June 2018

Cancellation by sponsor

Requested by Eli Lilly Australia Pty Ltd
HUMALOG NPL KwikPen insulin lispro 100U/mL injection multidose syringe Cancelled under Section 30(1)(c) of the Act

29 June 2018

Cancellation by sponsor

Requested by Eli Lilly Australia Pty Ltd
TRENUVIS pemetrexed (as disodium) 100 mg powder for injection vial Cancelled under Section 30(1)(c) of the Act

29 June 2018

Cancellation by sponsor

Requested by Eli Lilly Australia Pty Ltd
TRENUVIS pemetrexed (as disodium) 500mg powder for injection vial Cancelled under Section 30(1)(c) of the Act

29 June 2018

Cancellation by sponsor

Requested by Eli Lilly Australia Pty Ltd
TALTZ (Eli Lilly Australia Pty Ltd)

22 June 2018

Prescription medicine registration

Active ingredients: ixekizumab.

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The Department of Health, Disability and Ageing acknowledges First Nations peoples as the Traditional Owners of Country throughout Australia, and their continuing connection to land, sea and community. We pay our respects to them and their cultures, and to all Elders both past and present.