01 12care4
02 1AOP Health
03 5Accord healthcare
04 1Alkermes Contract Pharma Services
05 1Arrotex Pharmaceuticals
06 1Bristol Myers Squibb
07 2Central Procurement & Supplies Unit
08 1Currax
09 1Ebb Medical
10 1Generic Health
11 1Health House Pharma Ltd T/As P&D Pharmaceuticals Ltd
12 2Intas Pharmaceuticals
13 1L Molteni & C Dei F.Lli Alitti Spa Operating Company
14 1Molteni Farmaceutici
15 1NANO DARU
16 3ORIFARM GROUP AS
17 1OrPha Swiss
18 1P & D Pharmaceuticals Limited
19 3POA Pharma
20 1Paranova Pharmaceuticals Ab
21 1Pharmathen SA
22 1Prohealth Limited
23 1Teva Pharmaceutical Industries
24 1Unimedic AB
01 1Extended Release Injectable Suspension
02 2FOR SUSPENSION, EXTENDED RELEASE;INTRAMUSCULAR
03 14Film Coated Tablet
04 1Film Coated Tablet
05 1Film-Coated Tablet
06 2Film-Coated Tablets
07 1Long Acting Injectable
08 1PR Tablet
09 9Tablet
10 2tablet
01 1Allowed
02 4Approved
03 2Authorised
04 1DISCN
05 9Deregistered
06 2Invalid
07 2Marketed
08 2Prescription
09 1RX
10 2Withdrawn
11 8Blank
01 1ARX-NALTREXONE
02 1Destoxican
03 1Mysimba
04 1NALOREX
05 1NALTREXONE
06 1NALTREXONE ACCORD HEALTHCARE
07 1Nalorex
08 1Naltrexine
09 1Naltrexon Ebb
10 1Naltrexon Molteni
11 1Naltrexon Vitaflo
12 1Naltrexone 2Care4
13 3Naltrexone Accord
14 1Naltrexone Accord Healthcare
15 1Naltrexone GH
16 3Naltrexone Hydrochloride
17 1Naltrexone POA Pharma
18 2Naltrexone Poa Pharma
19 6Revia
20 1VIVITROL
21 4Blank
01 2Australia
02 2Estonia
03 1Greece
04 2India
05 1Iran
06 2Italy
07 6Malta
08 2Norway
09 13Sweden
10 1Switzerland
11 2USA
Regulatory Info :
Registration Country : Italy
Brand Name : NALTREXONE ACCORD HEALTHCARE
Dosage Form : Film-Coated Tablets
Dosage Strength : 50 mg
Packaging : 14 UNITS 50 MG - ORAL USE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : Withdrawn
Registration Country : Malta
Brand Name : Naltrexone Hydrochloride
Dosage Form : Film Coated Tablet
Dosage Strength : 50MG
Packaging :
Approval Date : 2016-04-12
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta
Regulatory Info : Marketed
Registration Country : Norway
Brand Name : Naltrexone Accord
Dosage Form : Film Coated Tablet
Dosage Strength : 50mg
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway
Regulatory Info : Prescription
Registration Country : Estonia
Brand Name : Naltrexone Accord
Dosage Form : Film-Coated Tablet
Dosage Strength : 50mg
Packaging :
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Estonia
Regulatory Info : RX
Registration Country : USA
Brand Name : VIVITROL
Dosage Form : FOR SUSPENSION, EXTENDED RELEASE;INTRAMUSCULAR
Dosage Strength : 380MG/VIAL
Packaging :
Approval Date : 2006-04-13
Application Number : 21897
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Revia
Dosage Form : Tablet
Dosage Strength : 50mg
Packaging :
Approval Date : 10-03-2000
Application Number : 2.00E+13
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Prescription
Registration Country : Estonia
Brand Name : Mysimba
Dosage Form : Tablet
Dosage Strength : 90mg; 8mg
Packaging :
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Estonia
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : PR Tablet
Dosage Strength : 8MG; 90MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Film Coated Tablet
Dosage Strength : 50MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : Italy
Brand Name : NALOREX
Dosage Form : Film-Coated Tablets
Dosage Strength : 50 mg
Packaging : 14 UNITS 50 MG - ORAL USE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Iran
Brand Name :
Dosage Form : Extended Release Injectable Suspension
Dosage Strength : 380Mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Iran
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Naltrexine
Dosage Form : Film Coated Tablet
Dosage Strength : 45.2mg
Packaging :
Approval Date : 22/04/2003
Application Number : 56109
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info :
Registration Country : Greece
Brand Name :
Dosage Form : Long Acting Injectable
Dosage Strength : 380MG/VIAL
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Greece
Regulatory Info : Marketed
Registration Country : Norway
Brand Name : Naltrexone POA Pharma
Dosage Form : Film Coated Tablet
Dosage Strength : 50mg
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NALTREXONE
Dosage Form : FOR SUSPENSION, EXTENDED RELEASE;INTRAMUSCULAR
Dosage Strength : 380MG/VIAL
Packaging :
Approval Date : 2023-07-06
Application Number : 213195
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Withdrawn
Registration Country : Malta
Brand Name : Nalorex
Dosage Form : Tablet
Dosage Strength : 50MG
Packaging :
Approval Date : 2008-03-11
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : Invalid
Registration Country : Malta
Brand Name : Naltrexone Hydrochloride
Dosage Form : Film Coated Tablet
Dosage Strength : 50MG
Packaging :
Approval Date : 2019-08-26
Application Number :
Regulatory Info : Invalid
Registration Country : Malta
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : Invalid
Registration Country : Malta
Brand Name : Naltrexone Hydrochloride
Dosage Form : Film Coated Tablet
Dosage Strength : 50MG
Packaging :
Approval Date : 2019-11-22
Application Number :
Regulatory Info : Invalid
Registration Country : Malta
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : Authorised
Registration Country : Malta
Brand Name : Destoxican
Dosage Form : Tablet
Dosage Strength : 50MG
Packaging :
Approval Date : 2022-11-22
Application Number :
Regulatory Info : Authorised
Registration Country : Malta
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : Authorised
Registration Country : Malta
Brand Name : Naltrexone Accord Healthcare
Dosage Form : Film Coated Tablet
Dosage Strength : 50MG; 50MG
Packaging :
Approval Date : 2020-10-22
Application Number :
Regulatory Info : Authorised
Registration Country : Malta
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
