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Southern Cross Pharma Pty Ltd

Regulatory activities for this sponsor.

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ARTG (260)
Cancellation by sponsor (204)
Prescription medicine registration (22)
Australian public assessment report (AusPar) (4)
Prescription medicine decision summary (1)
Section 14, TGO91 consent (1)

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Sponsor content

492 result(s) found, displaying 451 to 460

GALANTAMINE SZ galantamine (as hydrobromide) 16mg modified release capsules blister pack (182037)

20 January 2012

ARTG

Australian Register of Therapeutic Goods (ARTG) information for GALANTAMINE SZ galantamine (as hydrobromide) 16mg modified release capsules blister pack.
GALANTAMINE SR SCP galantamine (as hydrobromide) 24mg modified release capsules blister pack (182039)

20 January 2012

ARTG

Australian Register of Therapeutic Goods (ARTG) information for GALANTAMINE SR SCP galantamine (as hydrobromide) 24mg modified release capsules blister pack.
GALANTAMINE SR SCP galantamine (as hydrobromide) 16mg modified release capsules blister pack (182035)

20 January 2012

ARTG

Australian Register of Therapeutic Goods (ARTG) information for GALANTAMINE SR SCP galantamine (as hydrobromide) 16mg modified release capsules blister pack.
GALANTAMINE SR SCP galantamine (as hydrobromide) 8mg modified release capsules blister pack (182029)

20 January 2012

ARTG

Australian Register of Therapeutic Goods (ARTG) information for GALANTAMINE SR SCP galantamine (as hydrobromide) 8mg modified release capsules blister pack.
GALANTAMINE SZ galantamine (as hydrobromide) 24mg modified release capsules blister pack (182031)

20 January 2012

ARTG

Australian Register of Therapeutic Goods (ARTG) information for GALANTAMINE SZ galantamine (as hydrobromide) 24mg modified release capsules blister pack.
PEXEMIS pramipexole dihydrochloride monohydrate 0.125 mg tablet blister pack (172023)

25 October 2011

ARTG

Australian Register of Therapeutic Goods (ARTG) information for PEXEMIS pramipexole dihydrochloride monohydrate 0.125 mg tablet blister pack.
PEXEMIS pramipexole dihydrochloride monohydrate 0.25 mg tablet blister pack (172024)

25 October 2011

ARTG

Australian Register of Therapeutic Goods (ARTG) information for PEXEMIS pramipexole dihydrochloride monohydrate 0.25 mg tablet blister pack.
PEXEMIS pramipexole dihydrochloride monohydrate 1.5 mg tablet blister pack (172027)

25 October 2011

ARTG

Australian Register of Therapeutic Goods (ARTG) information for PEXEMIS pramipexole dihydrochloride monohydrate 1.5 mg tablet blister pack.
PEXEMIS pramipexole dihydrochloride monohydrate 0.5 mg tablet blister pack (172025)

25 October 2011

ARTG

Australian Register of Therapeutic Goods (ARTG) information for PEXEMIS pramipexole dihydrochloride monohydrate 0.5 mg tablet blister pack.
PEXEMIS pramipexole dihydrochloride monohydrate 1 mg tablet blister pack (172026)

25 October 2011

ARTG

Australian Register of Therapeutic Goods (ARTG) information for PEXEMIS pramipexole dihydrochloride monohydrate 1 mg tablet blister pack.

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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.