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Mundipharma Pty Ltd

Regulatory activities for this sponsor.

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Type

Cancellation by sponsor (127)
ARTG (90)
Australian Public Assessment Report (AusPAR) (9)
Prescription medicine registration (2)
Cancellation or suspension (1)

Date

2026 (9)
2025 (4)
2024 (16)
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2022 (62)
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2020 (28)
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1996 (1)
1995 (3)
1993 (3)
1991 (2)

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Sponsor content

229 result(s) found, displaying 151 to 160

TARGIN oxycodone hydrochloride / naloxone hydrochloride anhydrous 2.5/1.25mg modified release tablets blister pack (216260)

24 September 2014

ARTG

Australian Register of Therapeutic Goods (ARTG) information for TARGIN oxycodone hydrochloride / naloxone hydrochloride anhydrous 2.5/1.25mg modified release tablets blister pack.
TARGIN oxycodone hydrochloride / naloxone hydrochloride 30/15mg modified release tablets blister pack (216280)

24 September 2014

ARTG

Australian Register of Therapeutic Goods (ARTG) information for TARGIN oxycodone hydrochloride / naloxone hydrochloride 30/15mg modified release tablets blister pack.
TARGIN oxycodone hydrochloride / naloxone hydrochloride 15/7.5mg modified release tablets blister pack (216261)

24 September 2014

ARTG

Australian Register of Therapeutic Goods (ARTG) information for TARGIN oxycodone hydrochloride / naloxone hydrochloride 15/7.5mg modified release tablets blister pack.
DILAUDID-HP hydromorphone hydrochloride 10mg/1mL injection ampoule Cancelled under s30(1)(c) of the Act

8 February 2018

Cancellation by sponsor

Requested by Mundipharma Pty Ltd
DILAUDID-HP hydromorphone hydrochloride 50mg/5mL injection ampoule Cancelled under s30(1)(c)

4 August 2017

Cancellation by sponsor

Requested by Mundipharma Pty Ltd
OXYCONTIN oxycodone hydrochloride 5mg modified release tablet blister pack Cancelled under s30(1)(c)

30 June 2017

Cancellation by sponsor

Requested by Mundipharma Pty Ltd
OXYCONTIN oxycodone hydrochloride 15mg modified release tablet bottle Cancelled under s30(1)(c)

30 June 2017

Cancellation by sponsor

Requested by Mundipharma Pty Ltd
OXYCONTIN oxycodone hydrochloride 30mg modified release tablet bottle Cancelled under s30(1)(c)

30 June 2017

Cancellation by sponsor

Requested by Mundipharma Pty Ltd
OXYCONTIN oxycodone hydrochloride 60mg modified release tablet bottle Cancelled under s30(1)(c)

30 June 2017

Cancellation by sponsor

Requested by Mundipharma Pty Ltd
OXYCONTIN oxycodone hydrochloride 80mg modified release tablet bottle Cancelled under s30(1)(c)

30 June 2017

Cancellation by sponsor

Requested by Mundipharma 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.