Approvals/TGA/SUBUTEX FDT buprenorphine 16 mg (as hydrochloride) tablet blister pack

Approved

STANDARD

SUBUTEX FDT buprenorphine 16 mg (as hydrochloride) tablet blister pack

Indivior Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 43a1887550a5f9e2
Product Name: SUBUTEX FDT buprenorphine 16 mg (as hydrochloride) tablet blister pack
Artg Id: 134407
Artg Name: SUBUTEX FDT buprenorphine 16 mg (as hydrochloride) tablet blister pack
Sponsor: Indivior Pty Ltd
Company Detail Path: /organization/indivior-pty-ltd
Artg Date: 2007-10-31
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 29, 2025

Approval ID

43a1887550a5f9e2

Type

Standard