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Southern Cross Pharma Pty Ltd

Regulatory activities for this sponsor.

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Type

ARTG (259)
Cancellation by sponsor (204)
Prescription medicine registration (22)
Australian public assessment report (AusPar) (4)
Prescription medicine decision summary (1)
Section 14, TGO91 consent (1)

Date

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Sponsor content

491 result(s) found, displaying 221 to 230

MOMEX SR morphine sulfate as pentahydrate 30 mg tablet blister packs Cancelled under Section 30(1)(c) of the Act

22 June 2021

Cancellation by sponsor

Requested by Southern Cross Pharma Pty Ltd
MOMEX SR morphine sulfate as pentahydrate 100 mg tablet blister packs Cancelled under Section 30(1)(c) of the Act

22 June 2021

Cancellation by sponsor

Requested by Southern Cross Pharma Pty Ltd
MOMEX SR morphine sulfate as pentahydrate 60 mg tablet blister packs Cancelled under Section 30(1)(c) of the Act

22 June 2021

Cancellation by sponsor

Requested by Southern Cross Pharma Pty Ltd
TERRY WHITE CHEMISTS TRAMADOL SR tramadol hydrochloride 100 mg oral tablet blister pack Cancelled under Section 30(1)(c) of the Act

22 June 2021

Cancellation by sponsor

Requested by Southern Cross Pharma Pty Ltd
CHEMMART TRAMADOL SR tramadol hydrochloride 100 mg oral tablet blister pack Cancelled under Section 30(1)(c) of the Act

22 June 2021

Cancellation by sponsor

Requested by Southern Cross Pharma Pty Ltd
APO-FENOFIBRATE fenofibrate 48 mg tablet blister pack (291653)

17 May 2019

ARTG

Australian Register of Therapeutic Goods (ARTG) information for APO-FENOFIBRATE fenofibrate 48 mg tablet blister pack.
FENOFIBRATE SCP fenofibrate 145 mg tablet blister pack (291668)

17 May 2019

ARTG

Australian Register of Therapeutic Goods (ARTG) information for FENOFIBRATE SCP fenofibrate 145 mg tablet blister pack.
FENOFIBRATE SCP fenofibrate 48 mg tablet blister pack (291669)

17 May 2019

ARTG

Australian Register of Therapeutic Goods (ARTG) information for FENOFIBRATE SCP fenofibrate 48 mg tablet blister pack.
APO-FENOFIBRATE fenofibrate 145 mg tablet blister pack (291652)

17 May 2019

ARTG

Australian Register of Therapeutic Goods (ARTG) information for APO-FENOFIBRATE fenofibrate 145 mg tablet blister pack.
AusPAR: Labetalol hydrochloride

12 April 2021

Australian public assessment report (AusPar)

Australian Public Assessment Report for Labetalol hydrochloride

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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.