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Sun Pharma ANZ Pty Ltd

Regulatory activities for this sponsor.

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Type

ARTG (452)
Cancellation by sponsor (155)
Prescription medicine registration (29)
Section 14, TGO91 consent (5)
Australian public assessment report (AusPar) (4)
Prescription medicine decision summary (1)

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Sponsor content

646 result(s) found, displaying 251 to 260

ABISART 150 irbesartan 150 mg tablet blister pack (302143)

30 October 2018

ARTG

Australian Register of Therapeutic Goods (ARTG) information for ABISART 150 irbesartan 150 mg tablet blister pack.
ABISART 300 irbesartan 300 mg tablet blister pack (302144)

30 October 2018

ARTG

Australian Register of Therapeutic Goods (ARTG) information for ABISART 300 irbesartan 300 mg tablet blister pack.
ABISART 75 irbesartan 75 mg tablet blister pack (302142)

30 October 2018

ARTG

Australian Register of Therapeutic Goods (ARTG) information for ABISART 75 irbesartan 75 mg tablet blister pack.
SUNITINIB SUN (Sun Pharma ANZ Pty Ltd)

9 February 2021

Prescription medicine registration

Active ingredients: sunitinib malate.
ILUMYA tildrakizumab (rch) 100 mg/1 mL solution for injection pre-filled syringe (290683)

10 September 2018

ARTG

Australian Register of Therapeutic Goods (ARTG) information for ILUMYA tildrakizumab (rch) 100 mg/1 mL solution for injection pre-filled syringe.
LURASIDONE SUN (Sun Pharma ANZ Pty Ltd)

10 November 2020

Prescription medicine registration

Active ingredients: lurasidone hydrochloride.
GANIRELIX SUN (Sun Pharma ANZ Pty Ltd)

2 November 2020

Prescription medicine registration

Active ingredients: ganirelix acetate.
HYFORIL 10/12.5 mg fosinopril sodium10mg and hydrochlorothiazide 12.5mg tablet blister pack Cancelled under Section 30(1)(c) of the Act

4 September 2020

Cancellation by sponsor

Requested by Sun Pharma ANZ Pty Ltd
HYFORIL 10/12.5 mg fosinopril sodium 10mg and hydrochlorothiazide 12.5mg tablet bottle Cancelled under Section 30(1)(c) of the Act

4 September 2020

Cancellation by sponsor

Requested by Sun Pharma ANZ Pty Ltd
HYFORIL 20/12.5 mg fosinopril sodium 20mg and hydrochlorothiazide 12.5mg tablet blister pack Cancelled under Section 30(1)(c) of the Act

4 September 2020

Cancellation by sponsor

Requested by Sun Pharma ANZ Pty Ltd

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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.