The government is now operating in accordance with the Guidance on Caretaker Conventions, pending the outcome of the 2025 federal election.
You are here Home Guidance and resources Cancellations and suspensions This database records details of medicines and medical devices that have been cancelled or suspended, and no longer appear in the ARTG. Listen Print Share Loading... Use the filters below to narrow your search. Filter results Open all Close all You can narrow down the results using the filters. Action Alphapharm Pty Ltd (1) (-) Alphapharm Pty Ltd (1) Medical device cancellation (832) Medical device cancellation (832) Medicine suspension (506) Medicine suspension (506) Complementary medicine cancellation (203) Complementary medicine cancellation (203) Medical device suspension (86) Medical device suspension (86) Medicine cancellation (59) Medicine cancellation (59) Revocation of a TGA issued Conformity Assessment Certificate (51) Revocation of a TGA issued Conformity Assessment Certificate (51) Medical device cancellation - certain devices within an entry (23) Medical device cancellation - certain devices within an entry (23) Registered medicine cancellation (12) Registered medicine cancellation (12) Voluntary revocation at the request of the manufacturer (9) Voluntary revocation at the request of the manufacturer (9) Medical device cancellation - requested by the sponsor - certain devices within an entry (8) Medical device cancellation - requested by the sponsor - certain devices within an entry (8) Medical device cancellation (7) Medical device cancellation (7) Listed medicine cancellation (3) Listed medicine cancellation (3) Listed medicine cancellation (3) Listed medicine cancellation (3) Revocation of a TGA issued Conformity Assessment Certificate. (3) Revocation of a TGA issued Conformity Assessment Certificate. (3) Revocation of medical device suspension (2) Revocation of medical device suspension (2) Revoked medicine suspension (2) Revoked medicine suspension (2) AFT Pharmaceuticals Pty Ltd (1) AFT Pharmaceuticals Pty Ltd (1) Medical device cancellation (1) Medical device cancellation (1) Suspension from the ARTG under subsection s41GA(1)(b) (1) Suspension from the ARTG under subsection s41GA(1)(b) (1) Voluntary revocation at the request of the manufacturer. (1) Voluntary revocation at the request of the manufacturer. (1) Date of effect 2024 (1) 2024 (1) Find out more about Cancellations and Suspensions. Search Filters applied:Alphapharm Pty LtdClear all Search1 result(s) found, displaying 1 to 1 RANI 2 ranitidine 300mg (as hydrochloride) tablet blister pack (Suspension effective for 6 months. A decision was made to extend the suspension for a further 6 months in accordance with section 29E of the Act. ) 17 December 2024 Cancellation or suspension Regulatory action due to , effective 17/12/2024
RANI 2 ranitidine 300mg (as hydrochloride) tablet blister pack (Suspension effective for 6 months. A decision was made to extend the suspension for a further 6 months in accordance with section 29E of the Act. ) 17 December 2024 Cancellation or suspension Regulatory action due to , effective 17/12/2024