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01 2H. Lundbeck

02 5H. Lundbeck A/S

03 1Lundbeck (Switzerland) Ag

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PharmaCompass

01

Asia Pharma Expo
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Nalmefene Hydrochloride Dihydrate

Brand Name : Selincro

Dosage Form : Film Coated Tablet

Dosage Strength : 18mg

Packaging :

Approval Date : 25/02/2013

Application Number : 20120120000033

Regulatory Info : Approved

Registration Country : Sweden

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02

Asia Pharma Expo
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Asia Pharma Expo
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Nalmefene

Brand Name : Selincro

Dosage Form : Film Coated Tablet

Dosage Strength : 186mg

Packaging :

Approval Date : 15/04/2014

Application Number : 62764

Regulatory Info : Allowed

Registration Country : Switzerland

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03

Asia Pharma Expo
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Asia Pharma Expo
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Nalmefene hydrochloride dihydrate

Brand Name : Selincro

Dosage Form : Film Coated Tablet

Dosage Strength : 18mg

Packaging :

Approval Date :

Application Number :

Regulatory Info : Marketed

Registration Country : Norway

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04

Asia Pharma Expo
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Asia Pharma Expo
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Nalmefene hydrochloride dihydrate

Brand Name : Selincro

Dosage Form : Film Coated Tablet

Dosage Strength : 18mg

Packaging :

Approval Date :

Application Number :

Regulatory Info : Marketed

Registration Country : Norway

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05

Asia Pharma Expo
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Asia Pharma Expo
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nalmefene

Brand Name : Selincro

Dosage Form : Film-Coated Tablet

Dosage Strength : 18mg

Packaging :

Approval Date :

Application Number :

Regulatory Info : Prescription

Registration Country : Estonia

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06

Asia Pharma Expo
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Asia Pharma Expo
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Nalmefene

Brand Name : Selincro

Dosage Form : Film Coated Tablet

Dosage Strength : 18MG

Packaging :

Approval Date : 30-04-2013

Application Number : 112815002

Regulatory Info : Authorized

Registration Country : Spain

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07

Asia Pharma Expo
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Asia Pharma Expo
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Nalmefene

Brand Name : Selincro

Dosage Form : Film Coated Tablet

Dosage Strength : 18MG

Packaging :

Approval Date : 20-11-2024

Application Number : 112815002IP

Regulatory Info : Authorized

Registration Country : Spain

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08

Asia Pharma Expo
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Asia Pharma Expo
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Nalmefene Hydrochloride Dihydrate

Brand Name : Selincro

Dosage Form : Film Coated Tablet

Dosage Strength : 18mg

Packaging :

Approval Date : 25-02-2013

Application Number : 28105020012

Regulatory Info : Prescription

Registration Country : Denmark

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