TGA Approval

MPL- OXYCODONE/NALOXONE oxycodone hydrochloride / naloxone hydrochloride 40/20 mg modified release tablet blister pack (288270)

ARTG ID

288270

ARTG Name

MPL- OXYCODONE/NALOXONE oxycodone hydrochloride / naloxone hydrochloride 40/20 mg modified release tablet blister pack

Sponsor

Mundipharma Pty Ltd

ARTG Date

October 17, 2022

Registration Type

Medicine

Therapeutic Good Type

Medicine

Licence Status

Active

Licence Category

Registered

Sponsor Information

Sponsor Name

Sponsor Item Name

Mundipharma Pty Ltd.

Ingredient Name

naloxone hydrochloride dihydrate

Ingredient Name

oxycodone hydrochloride

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MPL- OXYCODONE/NALOXONE oxycodone hydrochloride / naloxone hydrochloride 40/20 mg modified release tablet blister pack (288270) - TGA 批准文号 | MedPath