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01 2Rusan Pharma

02 12care4

03 4Accord healthcare

04 1Acino Pharma

05 6Actavis Inc

06 1Apotex Inc

07 1Barr Laboratories

08 1Bausch Health

09 1Bristol Myers Squibb

10 1Chartwell Pharmaceuticals llc

11 1Currax

12 1Elite Laboratories

13 4Mallinckrodt Pharmaceuticals

14 1Molteni Farmaceutici

15 1Novitium Pharma LLC

16 1ORIFARM GROUP AS

17 2Orexigen Therapeutics Ireland Limited

18 1Orexigen Therapeutics Ireland Limited (1)

19 6Pfizer Inc

20 1Pluviaendo

21 1SIRTON MEDICARE Srl

22 1Sterinova Inc.

23 1Sun Pharmaceutical Industries Limited

24 2Teva Pharmaceutical Industries

25 2Zambon Switzerland

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothRusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.

Regulatory Info :

Registration Country : India

Naltrexone Hydrochloride

Brand Name : Naltrexone Hydrochloride

Dosage Form : Tablet

Dosage Strength : 50mg

Packaging : Pack Size 3x10; 2x14; 10x10

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Rusan Pharma

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothRusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.

Regulatory Info :

Registration Country : India

Naltrexone Hydrochloride

Brand Name : Naltrexone Hydrochloride

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

Rusan Pharma

03

SCOPE Summit
Not Confirmed
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SCOPE Summit
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NALTREXONE HYDROCHLORIDE

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

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04

SCOPE Summit
Not Confirmed
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SCOPE Summit
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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Dosage Strength : 20MG;0.8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

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05

SCOPE Summit
Not Confirmed
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SCOPE Summit
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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

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06

SCOPE Summit
Not Confirmed
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SCOPE Summit
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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

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07

SCOPE Summit
Not Confirmed
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SCOPE Summit
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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

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08

SCOPE Summit
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SCOPE Summit
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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

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09

SCOPE Summit
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SCOPE Summit
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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

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10

SCOPE Summit
Not Confirmed
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SCOPE Summit
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NALTREXONE HYDROCHLORIDE

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

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11

SCOPE Summit
Not Confirmed
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SCOPE Summit
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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

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12

SCOPE Summit
Not Confirmed
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SCOPE Summit
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NALTREXONE HYDROCHLORIDE

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

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13

SCOPE Summit
Not Confirmed
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SCOPE Summit
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NALTREXONE HYDROCHLORIDE

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

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14

SCOPE Summit
Not Confirmed
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SCOPE Summit
Not Confirmed

NALTREXONE HYDROCHLORIDE

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

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15

SCOPE Summit
Not Confirmed
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SCOPE Summit
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NALTREXONE HYDROCHLORIDE

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

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16

SCOPE Summit
Not Confirmed
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SCOPE Summit
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NALTREXONE HYDROCHLORIDE

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

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17

SCOPE Summit
Not Confirmed
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SCOPE Summit
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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

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18

SCOPE Summit
Not Confirmed
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SCOPE Summit
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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

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19

SCOPE Summit
Not Confirmed
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SCOPE Summit
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NALTREXONE HYDROCHLORIDE

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

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20

SCOPE Summit
Not Confirmed
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SCOPE Summit
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NALTREXONE HYDROCHLORIDE

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

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