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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)

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Sponsor content

646 result(s) found, displaying 381 to 390

FRUSEMIDE RBX furosemide (frusemide) 40 mg tablet bottle Cancelled under Section 30(1)(c) of the Act

27 March 2018

Cancellation by sponsor

Requested by Sun Pharma ANZ Pty Ltd
FRUSEMIDE RBX furosemide (frusemide) 20 mg tablet bottle Cancelled under Section 30(1)(c) of the Act

27 March 2018

Cancellation by sponsor

Requested by Sun Pharma ANZ Pty Ltd
CLOPIDOGREL RBX clopidogrel (as hydrogen sulfate) 75 mg tablet blister pack Cancelled under Section 30(1)(c) of the Act

27 March 2018

Cancellation by sponsor

Requested by Sun Pharma ANZ Pty Ltd
IRBESARTAN/HCTZ RBX 300/25 irbesartan 300 mg + hydrochlorothiazide 25 mg tablet blister pack Cancelled under Section 30(1)(c) of the Act

27 March 2018

Cancellation by sponsor

Requested by Sun Pharma ANZ Pty Ltd
IRBESARTAN/HCTZ RBX 150/12.5 irbesartan 150 mg + hydrochlorothiazide 12.5 mg tablet blister pack Cancelled under Section 30(1)(c) of the Act

27 March 2018

Cancellation by sponsor

Requested by Sun Pharma ANZ Pty Ltd
IRBESARTAN RBX irbesartan 150 mg tablet blister pack Cancelled under Section 30(1)(c) of the Act

27 March 2018

Cancellation by sponsor

Requested by Sun Pharma ANZ Pty Ltd
IRBESARTAN RBX irbesartan 300 mg tablet blister pack Cancelled under Section 30(1)(c) of the Act

27 March 2018

Cancellation by sponsor

Requested by Sun Pharma ANZ Pty Ltd
SEBIFIN terbinafine (as hydrochloride) 250 mg tablet blister pack Cancelled under s30(1)(c) of the Act

5 February 2018

Cancellation by sponsor

Requested by Sun Pharma ANZ Pty Ltd
DONEPEZIL GENERICHEALTH donepezil hydrochloride (as monohydrate) 10 mg tablet blister pack Cancelled under s30(1)(c) of the Act

5 February 2018

Cancellation by sponsor

Requested by Sun Pharma ANZ Pty Ltd
CEFACLOR SUN cefaclor 250mg/5mL (as monohydrate) powder for oral liquid bottle (226401)

2 September 2014

ARTG

Australian Register of Therapeutic Goods (ARTG) information for CEFACLOR SUN cefaclor 250mg/5mL (as monohydrate) powder for oral liquid bottle.

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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.