Faran Shimi: Leading producer of high-quality APIs & alkaloid opiates, serving major pharmaceutical companies across the Middle East.
01 1Faran Shimi Pharmaceutical
02 2Rusan Pharma
03 1AOP Orphan
04 4Accord healthcare
05 1Acino Pharma (Pty) Ltd
06 6Actavis Inc
07 1Advanz Pharma
08 1Apotex Inc
09 1Barr Laboratories
10 1Bausch Health
11 1Chartwell Pharmaceuticals llc
12 1Currax
13 1Elite Laboratories
14 1Fosun Pharmaceutical
15 4Mallinckrodt Pharmaceuticals
16 1Molteni Farmaceutici
17 1OrPha Swiss
18 1Orexigen Therapeutics Ireland Limited (1)
19 2POA Pharma Scandinavia AB
20 6Pfizer Inc
21 1Pluviaendo
22 1SIRTON MEDICARE Srl
23 1Sterinova Inc.
24 1Sun Pharmaceutical Industries Limited
25 2Teva Pharmaceutical Industries
26 2Zambon Switzerland
27 2Blank
01 1Antic-calc Tablet, Film Coated
02 12CAPSULE, EXTENDED RELEASE;ORAL
03 2Capsule
04 1Coated Tablet
05 1Depot tablet
06 4FILM COATED PILL
07 1Film Coated Tablet
08 1Filmtabl
09 2Naltrexone 50Mg 10 Units Oral Use
10 3Naltrexone 50Mg 14 Joined' Oral Use
11 1TAB
12 3TABLET
13 1TABLET (EXTENDED-RELEASE)
14 1TABLET, EXTENDED RELEASE;ORAL
15 10TABLET;ORAL
16 1Tab
17 2Tablet
18 1Tablet Implant
01 14DISCN
02 1Generic
03 1Originator
04 4Prescription
05 9RX
06 19Blank
01 128 Accord Naltrexone 50Mg Film-Coated Tablets Efg
02 1APO-NALTREXONE
03 2Antaxone
04 2CONTRAVE
05 1Contrave
06 6EMBEDA
07 1Mysimba
08 9NALTREXONE HYDROCHLORIDE
09 1NALTREXONE HYDROCHLORIDE TABLETS USP
10 1Nalorex
11 1Naltima
12 1Naltrexin
13 1Naltrexone
14 1Naltrexone Abcur
15 1Naltrexone Accord
16 2Naltrexone POA Pharma
17 1Narcoral
18 1Opizone
19 2REVIA
20 1Revia 50Mg 28 Coated Tablets
21 6TROXYCA ER
22 5Blank
01 4Canada
02 2India
03 1Iran
04 5Italy
05 2Norway
06 2South Africa
07 2Spain
08 4Sweden
09 1Switzerland
10 1Turkey
11 1U.S.A
12 23USA
Faran Shimi: Leading producer of high-quality APIs & alkaloid opiates, serving major pharmaceutical companies across the Middle East.
Regulatory Info :
Registration Country : Iran
Brand Name :
Dosage Form : Capsule
Dosage Strength : 50MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Iran
Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Tablet
Dosage Strength : 50mg
Packaging : Pack Size 3x10; 2x14; 10x10
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Tablet Implant
Dosage Strength : 765mg
Packaging : Pack Size 2 Tablets in 1 Carton; 1 Tablets in 1 Carton
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : RX
Registration Country : USA
Brand Name : NALTREXONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 2011-08-17
Application Number : 91205
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : Sweden
Brand Name : Naltrexone Accord
Dosage Form : FILM COATED PILL
Dosage Strength : 50 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info : DISCN
Registration Country : USA
MORPHINE SULFATE; NALTREXONE HYDROCHLORIDE
Brand Name : EMBEDA
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 20MG;0.8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2009-08-13
Application Number : 22321
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
MORPHINE SULFATE; NALTREXONE HYDROCHLORIDE
Brand Name : EMBEDA
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 30MG;1.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2009-08-13
Application Number : 22321
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
MORPHINE SULFATE; NALTREXONE HYDROCHLORIDE
Brand Name : EMBEDA
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 50MG;2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2009-08-13
Application Number : 22321
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
MORPHINE SULFATE; NALTREXONE HYDROCHLORIDE
Brand Name : EMBEDA
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 60MG;2.4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2009-08-13
Application Number : 22321
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
MORPHINE SULFATE; NALTREXONE HYDROCHLORIDE
Brand Name : EMBEDA
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 80MG;3.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2009-08-13
Application Number : 22321
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
MORPHINE SULFATE; NALTREXONE HYDROCHLORIDE
Brand Name : EMBEDA
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 100MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2009-08-13
Application Number : 22321
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : Sweden
Brand Name : Naltrexone Abcur
Dosage Form : FILM COATED PILL
Dosage Strength : 50 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Opizone
Dosage Form : FILM COATED PILL
Dosage Strength : 50 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info : RX
Registration Country : USA
Brand Name : NALTREXONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 1998-05-08
Application Number : 74918
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NALTREXONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 2017-07-21
Application Number : 207905
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
BUPROPION HYDROCHLORIDE; NALTREXONE HYDROCHLORIDE
Brand Name : CONTRAVE
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 90MG;8MG
Packaging :
Approval Date : 2014-09-10
Application Number : 200063
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NALTREXONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 1999-05-26
Application Number : 75274
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NALTREXONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 2000-03-08
Application Number : 75434
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NALTREXONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG
Packaging :
Approval Date : 2002-03-22
Application Number : 76264
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NALTREXONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 2002-03-22
Application Number : 76264
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NALTREXONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 100MG
Packaging :
Approval Date : 2002-03-22
Application Number : 76264
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
NALTREXONE HYDROCHLORIDE; OXYCODONE HYDROCHLORIDE
Brand Name : TROXYCA ER
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 1.2MG;10MG
Packaging :
Approval Date : 2016-08-19
Application Number : 207621
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
NALTREXONE HYDROCHLORIDE; OXYCODONE HYDROCHLORIDE
Brand Name : TROXYCA ER
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 2.4MG;20MG
Packaging :
Approval Date : 2016-08-19
Application Number : 207621
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
NALTREXONE HYDROCHLORIDE; OXYCODONE HYDROCHLORIDE
Brand Name : TROXYCA ER
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 3.6MG;30MG
Packaging :
Approval Date : 2016-08-19
Application Number : 207621
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
NALTREXONE HYDROCHLORIDE; OXYCODONE HYDROCHLORIDE
Brand Name : TROXYCA ER
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 4.8MG;40MG
Packaging :
Approval Date : 2016-08-19
Application Number : 207621
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
NALTREXONE HYDROCHLORIDE; OXYCODONE HYDROCHLORIDE
Brand Name : TROXYCA ER
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 7.2MG;60MG
Packaging :
Approval Date : 2016-08-19
Application Number : 207621
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
NALTREXONE HYDROCHLORIDE; OXYCODONE HYDROCHLORIDE
Brand Name : TROXYCA ER
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 9.6MG;80MG
Packaging :
Approval Date : 2016-08-19
Application Number : 207621
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NALTREXONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 2012-02-24
Application Number : 90356
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : REVIA
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 1984-11-20
Application Number : 18932
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : Sweden
Brand Name : Naltrexone POA Pharma
Dosage Form : FILM COATED PILL
Dosage Strength : 50 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
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