Cancellations requested by the sponsor - regulatory actions

Sponsors can submit requests to cancel entries in the Australian Register of Therapeutic Goods (ARTG). The Therapeutic Goods Act 1989 (the Act) requires the TGA to publish information on the Secretary’s decision to action these cancellations.

The cancellation provisions relating to cancellations requested by the sponsor in the Act are:

  • cancellation of listed or registered therapeutic goods: section 30(1)(c)
  • cancellation of biologicals: section 32GA(1)(d)
  • cancellation of medical devices: section 41GL(d).

The records below include information on the cancellation decisions and any subsequent decisions to revoke such cancellations. To find out whether a product is currently authorised for supply in Australia, check the ARTG.

Enter a product name or an ARTG number.

Cancellations

Displaying 61 - 70 of 19776

Lupin Australia Pty Limited

Product: PERINDOPRIL CH perindopril erbumine 2mg tablet blister pack

ARTG number: 125447

Type of decision: Cancelled under Section 30(1)(c) of the Act

Date of effect: 29 Jun 2018

Sandoz Pty Ltd

Product: GLIMEPIRIDE SANDOZ glimepiride 4 mg tablet bottle

ARTG number: 121791

Type of decision: Cancelled under Section 30(1)(c) of the Act

Date of effect: 29 Jun 2018

Sandoz Pty Ltd

Product: GLIMEPIRIDE SANDOZ glimepiride 3 mg tablet bottle

ARTG number: 121789

Type of decision: Cancelled under Section 30(1)(c) of the Act

Date of effect: 29 Jun 2018

Sandoz Pty Ltd

Product: GLIMEPIRIDE SANDOZ glimepiride 2 mg tablet bottle

ARTG number: 121787

Type of decision: Cancelled under Section 30(1)(c) of the Act

Date of effect: 29 Jun 2018

Sandoz Pty Ltd

Product: GLIMEPIRIDE SANDOZ glimepiride 1 mg tablet bottle

ARTG number: 121785

Type of decision: Cancelled under Section 30(1)(c) of the Act

Date of effect: 29 Jun 2018

Sandoz Pty Ltd

Product: QUINAPRIL SANDOZ quinapril 20mg (as hydrochloride) film coated tablets blister pack

ARTG number: 117226

Type of decision: Cancelled under Section 30(1)(c) of the Act

Date of effect: 29 Jun 2018

Sandoz Pty Ltd

Product: LEVO/CARBIDOPA SANDOZ levodopa and carbidopa monohydrate tablet blister pack

ARTG number: 99119

Type of decision: Cancelled under Section 30(1)(c) of the Act

Date of effect: 29 Jun 2018

Sandoz Pty Ltd

Product: AMOXYCLAV GH 875/125 amoxicillin 875mg (as trihydrate) & clavulanic acid 125mg (as potassium) tablet strip pack

ARTG number: 82832

Type of decision: Cancelled under Section 30(1)(c) of the Act

Date of effect: 29 Jun 2018

Sandoz Pty Ltd

Product: PAROXETINE SANDOZ paroxetine (as hydrochloride) 20mg tablet bottle

ARTG number: 82550

Type of decision: Cancelled under Section 30(1)(c) of the Act

Date of effect: 29 Jun 2018

Sandoz Pty Ltd

Product: MEDROXYPROGESTERONE SANDOZ medroxyprogesterone acetate 10mg tablet blister pack

ARTG number: 79252

Type of decision: Cancelled under Section 30(1)(c) of the Act

Date of effect: 29 Jun 2018

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