MedPath

RECORDATI RARE DISEASES AUSTRALIA PTY. LTD.

🇦🇺Australia
Ownership
-
Employees
-
Market Cap
-
Website

Clinical Trials

0

Active:0
Completed:0

Trial Phases

0 Phases

Drug Approvals

17

TGA:17

Drug Approvals

ISTURISA osilodrostat (as phosphate) 5 mg film-coated tablet blister pack (369218)

Product Name
ISTURISA osilodrostat (as phosphate) 5 mg film-coated tablet blister pack
Approval Date
May 12, 2022
TGA

ISTURISA osilodrostat (as phosphate) 10 mg film-coated tablet blister pack (369219)

Product Name
ISTURISA osilodrostat (as phosphate) 10 mg film-coated tablet blister pack
Approval Date
May 12, 2022
TGA

ISTURISA osilodrostat (as phosphate) 1 mg film-coated tablet blister pack (369220)

Product Name
ISTURISA osilodrostat (as phosphate) 1 mg film-coated tablet blister pack
Approval Date
May 12, 2022
TGA

CYSTADROPS - mercaptamine (cysteamine) (as hydrochloride) 3.8 mg/mL eye drops solution vial (351010)

Product Name
CYSTADROPS - mercaptamine (cysteamine) (as hydrochloride) 3.8 mg/mL eye drops solution vial
Approval Date
Jan 28, 2022
TGA

QARZIBA dinutuximab beta 4.5 mg/mL concentrate for solution for infusion, 20 mg/4.5 mL vial (321016)

Product Name
QARZIBA dinutuximab beta 4.5 mg/mL concentrate for solution for infusion, 20 mg/4.5 mL vial
Approval Date
Apr 2, 2020
TGA

PEDEA ibuprofen 10 mg/2 mL solution for intravenous infusion 2 mL glass ampoule (273093)

Product Name
PEDEA ibuprofen 10 mg/2 mL solution for intravenous infusion 2 mL glass ampoule
Approval Date
Mar 14, 2017
TGA

SYLVANT siltuximab (rmc) 100mg powder for injection vial (229996)

Product Name
SYLVANT siltuximab (rmc) 100mg powder for injection vial
Approval Date
Aug 31, 2015
TGA

SYLVANT siltuximab (rmc) 400mg powder for injection vial (229997)

Product Name
SYLVANT siltuximab (rmc) 400mg powder for injection vial
Approval Date
Aug 31, 2015
TGA

SIGNIFOR LAR pasireotide 20 mg (as embonate) modified release powder for injection vial and 2 mL diluent in prefilled syringe composite pack (225272)

Product Name
SIGNIFOR LAR pasireotide 20 mg (as embonate) modified release powder for injection vial and 2 mL diluent in prefilled syringe composite pack
Approval Date
May 4, 2015
TGA

SIGNIFOR LAR pasireotide 40 mg (as embonate) modified release powder for injection vial and 2 mL diluent in prefilled syringe composite pack (225273)

Product Name
SIGNIFOR LAR pasireotide 40 mg (as embonate) modified release powder for injection vial and 2 mL diluent in prefilled syringe composite pack
Approval Date
May 4, 2015
TGA
  • Prev
  • 1
  • 2
  • Next

Clinical Trials

No trials found

News

No news found

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.