Approvals/TGA/PHENTODUR phentermine (as hydrochloride) 40 mg modified release capsule blister pack

Approved

STANDARD

PHENTODUR phentermine (as hydrochloride) 40 mg modified release capsule blister pack

Arrotex Pharmaceuticals Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: d0b26cd0ebcf2726
Product Name: PHENTODUR phentermine (as hydrochloride) 40 mg modified release capsule blister pack
Artg Id: 310863
Artg Name: PHENTODUR phentermine (as hydrochloride) 40 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: https://medical-cdn.nocode.com/drug_tga/86722f3e2c9f16118a6986bbb1d3140a.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/05b5b2739bf436ed28060c7173dc000c.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

d0b26cd0ebcf2726

Type

Standard