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 41 - 50 of 18544

Symbion Pty Ltd

Product: CHEMMART PHARMACY STRONG PAIN WITH CALMATIVE tablets blister pack

ARTG number: 160497

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

Date of effect: 29 Jun 2018

Symbion Pty Ltd

Product: CHEMMART PHARMACY COLD & FLU PE tablets blister pack

ARTG number: 157754

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

Date of effect: 29 Jun 2018

Lupin Australia Pty Limited

Product: PERINDOPRIL AND INDAPAMIDE CH 4/1.25 perindopril erbumine 4mg and indapamide hemihydrate1.25mg tablet blister pack

ARTG number: 147136

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

Date of effect: 29 Jun 2018

Lupin Australia Pty Limited

Product: SERTRACOR 100 sertraline 100mg (as hydrochloride) tablet blister pack

ARTG number: 147078

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

Date of effect: 29 Jun 2018

Lupin Australia Pty Limited

Product: SERTRACOR 50 sertraline 50mg (as hydrochloride) tablet blister pack

ARTG number: 147077

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

Date of effect: 29 Jun 2018

Sigma Company Limited

Product: EVELEXA XR 150 venlafaxine (as hydrochloride) 150 mg extended release capsule blister pack

ARTG number: 146744

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

Date of effect: 29 Jun 2018

Sigma Company Limited

Product: EVELEXA XR 75 venlafaxine (as hydrochloride) 75 mg extended release capsule blister pack

ARTG number: 146729

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

Date of effect: 29 Jun 2018

Sigma Company Limited

Product: EVELEXA XR 37.5 venlafaxine (as hydrochloride) 37.5 mg modified release capsule blister pack

ARTG number: 146645

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

Date of effect: 29 Jun 2018

Sandoz Pty Ltd

Product: LAMOTRIGINE SZ lamotrigine 200 mg Dispersible/Chewable tablet blister pack

ARTG number: 143570

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

Date of effect: 29 Jun 2018

Sandoz Pty Ltd

Product: LAMOTRIGINE SZ lamotrigine 100 mg Dispersible/Chewable tablet blister pack

ARTG number: 143569

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

Date of effect: 29 Jun 2018

Pages