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Southern Cross Pharma Pty Ltd

Regulatory activities for this sponsor.

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Type

ARTG (263)
Cancellation by sponsor (201)
Prescription medicine registration (22)
Australian Public Assessment Report (AusPAR) (4)
Prescription medicine decision summary (1)
Section 14, TGO91 consent (1)

Date

2024 (16)
2023 (30)
2022 (102)
2021 (32)
2020 (52)
2019 (59)
2018 (35)
2017 (51)
2016 (22)
2015 (17)
2014 (9)
2013 (11)
2012 (19)
2011 (9)
2010 (10)
2009 (13)
2008 (3)
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2003 (1)

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492 result(s) found, displaying 361 to 370

PRAMIPEXOLE SCP pramipexole dihydrochloride monohydrate 0.5 mg tablet blister pack (227663)

17 November 2015

ARTG

Australian Register of Therapeutic Goods (ARTG) information for PRAMIPEXOLE SCP pramipexole dihydrochloride monohydrate 0.5 mg tablet blister pack.
PRAMIPEXOLE SCP pramipexole dihydrochloride monohydrate 1 mg tablet blister pack (227664)

17 November 2015

ARTG

Australian Register of Therapeutic Goods (ARTG) information for PRAMIPEXOLE SCP pramipexole dihydrochloride monohydrate 1 mg tablet blister pack.
APO-PRAMIPEXOLE pramipexole dihydrochloride monohydrate 1 mg tablet blister pack (227669)

17 November 2015

ARTG

Australian Register of Therapeutic Goods (ARTG) information for APO-PRAMIPEXOLE pramipexole dihydrochloride monohydrate 1 mg tablet blister pack.
PRAMIPEXOLE SCP pramipexole dihydrochloride monohydrate 1.5 mg tablet blister pack (227665)

17 November 2015

ARTG

Australian Register of Therapeutic Goods (ARTG) information for PRAMIPEXOLE SCP pramipexole dihydrochloride monohydrate 1.5 mg tablet blister pack.
APO-PRAMIPEXOLE pramipexole dihydrochloride monohydrate 0.125 mg tablet blister pack (227666)

17 November 2015

ARTG

Australian Register of Therapeutic Goods (ARTG) information for APO-PRAMIPEXOLE pramipexole dihydrochloride monohydrate 0.125 mg tablet blister pack.
APO-PRAMIPEXOLE pramipexole dihydrochloride monohydrate 0.25 mg tablet blister pack (227667)

17 November 2015

ARTG

Australian Register of Therapeutic Goods (ARTG) information for APO-PRAMIPEXOLE pramipexole dihydrochloride monohydrate 0.25 mg tablet blister pack.
BETAHISTINE SANDOZ betahistine dihydrochloride 16mg tablet blister pack (253732)

16 November 2015

ARTG

Australian Register of Therapeutic Goods (ARTG) information for BETAHISTINE SANDOZ betahistine dihydrochloride 16mg tablet blister pack.
TEMOZOLOMIDE AN temozolomide 5 mg capsule bottle Cancelled under Section 30(1)(c) of the Act

13 June 2018

Cancellation by sponsor

Requested by Southern Cross Pharma Pty Ltd
AMOXYCLAV AN 500/125 amoxicillin (as trihydrate) 500 mg and clavulanic acid (as potassium clavulanate) 125 mg tablet blister pack Cancelled under Section 30(1)(c) of the Act

13 June 2018

Cancellation by sponsor

Requested by Southern Cross Pharma Pty Ltd
AMOXYCLAV AN 875/125 amoxicillin (as trihydrate) 875 mg and clavulanic acid (as potassium clavulanate) 125 mg tablet blister pack Cancelled under Section 30(1)(c) of the Act

13 June 2018

Cancellation by sponsor

Requested by Southern Cross Pharma Pty Ltd

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The Department of Health and Aged Care 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.