Approvals/TGA/PHENTODUR phentermine (as hydrochloride) 30 mg modified release capsule blister pack

Approved

STANDARD

PHENTODUR phentermine (as hydrochloride) 30 mg modified release capsule blister pack

Arrotex Pharmaceuticals Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: db8ff376300f1308
Product Name: PHENTODUR phentermine (as hydrochloride) 30 mg modified release capsule blister pack
Artg Id: 310861
Artg Name: PHENTODUR phentermine (as hydrochloride) 30 mg modified release capsule blister pack
Sponsor: Arrotex Pharmaceuticals Pty Ltd
Company Detail Path: /organization/arrotex-pharmaceuticals-pty-ltd
Artg Date: 2021-08-11
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2023-CMI-02680-1
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2023-PI-02679-1

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

db8ff376300f1308

Type

Standard