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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)

Date

2026 (15)
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Sponsor content

646 result(s) found, displaying 221 to 230

YONSA MPRED (Sun Pharma ANZ Pty Ltd)

24 March 2022

Prescription medicine registration

Active ingredients: abiraterone acetate; methylprednisolone.
NOUMED PERINDOPRIL perindopril erbumine 4 mg tablet blister pack (324641)

6 February 2020

ARTG

Australian Register of Therapeutic Goods (ARTG) information for NOUMED PERINDOPRIL perindopril erbumine 4 mg tablet blister pack.
NOUMED PERINDOPRIL perindopril erbumine 2 mg tablet blister pack (324640)

6 February 2020

ARTG

Australian Register of Therapeutic Goods (ARTG) information for NOUMED PERINDOPRIL perindopril erbumine 2 mg tablet blister pack.
NOUMED PERINDOPRIL perindopril erbumine 8 mg tablet blister pack (324642)

6 February 2020

ARTG

Australian Register of Therapeutic Goods (ARTG) information for NOUMED PERINDOPRIL perindopril erbumine 8 mg tablet blister pack.
CEQUA ciclosporin 900 microgram/mL eye drops ampoule (313780)

31 January 2020

ARTG

Australian Register of Therapeutic Goods (ARTG) information for CEQUA ciclosporin 900 microgram/mL eye drops ampoule.
SITAGLIPTIN SUN (Sun Pharma ANZ Pty Ltd)

19 November 2021

Prescription medicine registration

Active ingredients: sitagliptin fumarate.
LEVOXINE (Sun Pharma ANZ Pty Ltd)

29 July 2021

Prescription medicine registration

Active ingredients: levothyroxine sodium.
OZIDAL risperidone 4mg tablet blister pack Cancelled under Section 30(1)(c) of the Act

30 June 2021

Cancellation by sponsor

Requested by Sun Pharma ANZ Pty Ltd
NOUMED VENLAFAXINE venlafaxine (as hydrochloride) 37.5 mg modified release capsule blister pack Cancelled under Section 30(1)(c) of the Act

30 June 2021

Cancellation by sponsor

Requested by Sun Pharma ANZ Pty Ltd
NOUMED VENLAFAXINE venlafaxine (as hydrochloride) 150 mg modified release capsule blister pack Cancelled under Section 30(1)(c) of the Act

30 June 2021

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.