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01 2Actavis Inc

02 3Bausch & Lomb Incorporated

03 8Bausch Health

04 1Curatis

05 2Link Healthcare

06 5Salix Pharmaceuticals

07 1TMC PHARMA SERVICE LTD

08 1US GENERICS, STERILES

09 1Viatris

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PharmaCompass

01

IPPE
Not Confirmed
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IPPE
Not Confirmed

METHYLNALTREXONE BROMIDE

Brand Name : METHYLNALTREXONE BROMIDE

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 8MG/0.4ML (8MG/0.4ML)

Packaging :

Approval Date : 2024-08-26

Application Number : 208112

Regulatory Info : DISCN

Registration Country : USA

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02

IPPE
Not Confirmed
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IPPE
Not Confirmed

METHYLNALTREXONE BROMIDE

Brand Name : METHYLNALTREXONE BROMIDE

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 12MG/0.6ML (12MG/0.6ML)

Packaging :

Approval Date : 2024-08-26

Application Number : 208112

Regulatory Info : DISCN

Registration Country : USA

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03

IPPE
Not Confirmed
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IPPE
Not Confirmed

Methylnaltrexone bromide

Brand Name : Relistor

Dosage Form : Solution For Injection

Dosage Strength : 12mg/0.6ml

Packaging :

Approval Date :

Application Number :

Regulatory Info : Marketed

Registration Country : Norway

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04

IPPE
Not Confirmed
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IPPE
Not Confirmed

Methylnaltrexone bromide

Brand Name : Relistor

Dosage Form : Solution For Injection

Dosage Strength : 12mg/0.6ml

Packaging :

Approval Date :

Application Number :

Regulatory Info : Marketed

Registration Country : Norway

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05

IPPE
Not Confirmed
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IPPE
Not Confirmed

Methylnaltrexone bromide

Brand Name : Relistor

Dosage Form : Solution For Injection

Dosage Strength : 12mg/0.6ml

Packaging :

Approval Date :

Application Number :

Regulatory Info : Marketed

Registration Country : Norway

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06

IPPE
Not Confirmed
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IPPE
Not Confirmed

Methylnaltrexone Bromide

Brand Name : Relistor

Dosage Form : Solution For Injection

Dosage Strength : 12mg

Packaging :

Approval Date : 06/09/2010

Application Number : 20090908000039

Regulatory Info : Approved

Registration Country : Sweden

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07

IPPE
Not Confirmed
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IPPE
Not Confirmed

Methylnaltrexone Bromide

Brand Name : Relistor

Dosage Form : Injectable Solution

Dosage Strength : 12mg/0.6ml

Packaging :

Approval Date : 02/07/2008

Application Number : 20070526000017

Regulatory Info : Approved

Registration Country : Sweden

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08

IPPE
Not Confirmed
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IPPE
Not Confirmed

Methylnaltrexone Bromide

Brand Name : Relistor

Dosage Form : Solution For Injection

Dosage Strength : 8mg

Packaging :

Approval Date : 06/09/2010

Application Number : 20090908000022

Regulatory Info : Approved

Registration Country : Sweden

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09

IPPE
Not Confirmed
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IPPE
Not Confirmed

Methylnaltrexone bromide

Brand Name : Relistor

Dosage Form : Solution For Injection

Dosage Strength : 12mg/0.6ml

Packaging :

Approval Date :

Application Number :

Regulatory Info : Prescription

Registration Country : Estonia

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10

IPPE
Not Confirmed
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IPPE
Not Confirmed

Methylnaltrexone Bromide

Brand Name : Relistor

Dosage Form : Solution For Injection

Dosage Strength : 12mg/0.6ml

Packaging :

Approval Date : 15/04/2009

Application Number : 58652

Regulatory Info : Allowed

Registration Country : Switzerland

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11

IPPE
Not Confirmed
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IPPE
Not Confirmed

Methylnaltrexone

Brand Name : Relistor

Dosage Form :

Dosage Strength :

Packaging : 1

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

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12

IPPE
Not Confirmed
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IPPE
Not Confirmed

Methylnaltrexone

Brand Name : Relistor

Dosage Form :

Dosage Strength :

Packaging : 7

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

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13

IPPE
Not Confirmed
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IPPE
Not Confirmed

METHYLNALTREXONE BROMIDE

Brand Name : RELISTOR

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 12MG/0.6ML (12MG/0.6ML)

Packaging :

Approval Date : 2008-04-24

Application Number : 21964

Regulatory Info : RX

Registration Country : USA

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14

IPPE
Not Confirmed
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IPPE
Not Confirmed

METHYLNALTREXONE BROMIDE

Brand Name : RELISTOR

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 8MG/0.4ML (8MG/0.4ML)

Packaging :

Approval Date : 2010-09-27

Application Number : 21964

Regulatory Info : RX

Registration Country : USA

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15

IPPE
Not Confirmed
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IPPE
Not Confirmed

METHYLNALTREXONE BROMIDE

Brand Name : RELISTOR

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 12MG/0.6ML (12MG/0.6ML)

Packaging :

Approval Date : 2010-09-27

Application Number : 21964

Regulatory Info : RX

Registration Country : USA

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16

IPPE
Not Confirmed
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IPPE
Not Confirmed

METHYLNALTREXONE BROMIDE

Brand Name : RELISTOR

Dosage Form : TABLET;ORAL

Dosage Strength : 150MG

Packaging :

Approval Date : 2016-07-19

Application Number : 208271

Regulatory Info : RX

Registration Country : USA

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17

IPPE
Not Confirmed
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IPPE
Not Confirmed

METHYLNALTREXONE BROMIDE

Brand Name : RELISTOR

Dosage Form : SOLUTION

Dosage Strength : 20MG/ML

Packaging : 0.6ML

Approval Date :

Application Number : 2308215

Regulatory Info : Prescription

Registration Country : Canada

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18

IPPE
Not Confirmed
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IPPE
Not Confirmed

METHYLNALTREXONE BROMIDE

Brand Name : METHYLNALTREXONE BROMIDE

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 12MG/0.6ML (12MG/0.6ML)

Packaging :

Approval Date : 2025-05-28

Application Number : 208592

Regulatory Info : DISCN

Registration Country : USA

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19

US GENERICS, STERILES

Country
IPPE
Not Confirmed
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US GENERICS, STERILES

Country
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IPPE
Not Confirmed

METHYLNALTREXONE BROMIDE

Brand Name : METHYLNALTREXONE BROMIDE

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 12MG/0.6ML

Packaging :

Approval Date :

Application Number : 208038

Regulatory Info :

Registration Country : USA

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20

TMC PHARMA SERVICE LTD

Country
IPPE
Not Confirmed
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TMC PHARMA SERVICE LTD

Country
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IPPE
Not Confirmed

Relistor

Brand Name : Relistor

Dosage Form : Metilnaltrexone 12Mg 7 Joined The Parenteral Use

Dosage Strength : 7 VIALS SC 12 mg 0.6 ml + 7 Syringes

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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