Approvals/TGA/BUPRADONE 2/0.5 buprenorphine (as hydrochloride) 2 mg and naloxone (as hydrochloride dihydrate) 0.5 mg sublingual tablet

Approved

STANDARD

BUPRADONE 2/0.5 buprenorphine (as hydrochloride) 2 mg and naloxone (as hydrochloride dihydrate) 0.5 mg sublingual tablet

Indivior Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 17d02e724506c4e1
Product Name: BUPRADONE 2/0.5 buprenorphine (as hydrochloride) 2 mg and naloxone (as hydrochloride dihydrate) 0.5 mg sublingual tablet
Artg Id: 152483
Artg Name: BUPRADONE 2/0.5 buprenorphine (as hydrochloride) 2 mg and naloxone (as hydrochloride dihydrate) 0.5 mg sublingual tablet
Sponsor: Indivior Pty Ltd
Company Detail Path: /organization/indivior-pty-ltd
Artg Date: 2008-09-09
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

17d02e724506c4e1

Type

Standard