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MPL- OXYCODONE/NALOXONE oxycodone hydrochloride / naloxone hydrochloride 10/5 mg modified release tablets blister pack
Approved
STANDARD
MPL- OXYCODONE/NALOXONE oxycodone hydrochloride / naloxone hydrochloride 10/5 mg modified release tablets blister pack
Mundipharma Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
4a88c2034e1acbe7
Company
Mundipharma Pty Ltd
Type
Standard
Approval Details
Approval Id
4a88c2034e1acbe7
Product Name
MPL- OXYCODONE/NALOXONE oxycodone hydrochloride / naloxone hydrochloride 10/5 mg modified release tablets blister pack
Artg Id
288266
Artg Name
MPL- OXYCODONE/NALOXONE oxycodone hydrochloride / naloxone hydrochloride 10/5 mg modified release tablets blister pack
Sponsor
Mundipharma Pty Ltd
Company Detail Path
/organization/mundipharma-pty-ltd
Artg Date
2022-10-17
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
4a88c2034e1acbe7
Type
Standard
Back to TGA Approvals
MPL- OXYCODONE/NALOXONE oxycodone hydrochloride / naloxone hydrochloride 10/5 mg modified release tablets blister pack - TGA Drug Approval Details
