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01 3Sichuan Qingmu Pharmaceutical

02 6H. Lundbeck AS

03 2Hikma Pharmaceuticals

04 1Indivior

05 2Purdue Pharmaceuticals L.P

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothQingmu Pharma: Patients first, FDA/CEP/US-DMF/US-VMF/ASMF APIs for Humans & Vets in 100+ countries.

Regulatory Info : RX

Registration Country : USA

NALMEFENE HYDROCHLORIDE

Brand Name : NALMEFENE HYDROCHLORIDE

Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

Dosage Strength : EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML)

Packaging :

Approval Date : 2023-11-15

Application Number : 216007

Regulatory Info : RX

Registration Country : USA

Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothQingmu Pharma: Patients first, FDA/CEP/US-DMF/US-VMF/ASMF APIs for Humans & Vets in 100+ countries.

Regulatory Info : RX

Registration Country : USA

NALMEFENE HYDROCHLORIDE

Brand Name : NALMEFENE HYDROCHLORIDE

Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

Dosage Strength : EQ 2MG BASE/2ML (EQ 1MG BASE/ML)

Packaging :

Approval Date : 2023-11-15

Application Number : 216007

Regulatory Info : RX

Registration Country : USA

Company Banner

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothQingmu Pharma: Patients first, FDA/CEP/US-DMF/US-VMF/ASMF APIs for Humans & Vets in 100+ countries.

Regulatory Info :

Registration Country : USA

NALMEFENE HYDROCHLORIDE

Brand Name : NALMEFENE HYDROCHLORIDE

Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

Dosage Strength : 2MG BASE/2ML (EQ 1MGBASE/ML)

Packaging :

Approval Date :

Application Number : 216007

Regulatory Info :

Registration Country : USA

Company Banner

04

SCI Medicinal Chemistry
Not Confirmed
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SCI Medicinal Chemistry
Not Confirmed

nalmefenhydrokloriddihydrat

Brand Name : Selincro

Dosage Form : FILM COATED PILL

Dosage Strength : 18 MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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05

SCI Medicinal Chemistry
Not Confirmed
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SCI Medicinal Chemistry
Not Confirmed

Nalmefene

Brand Name : Selincro

Dosage Form : Antic-calc Tablet, Film Coated

Dosage Strength : 18 mg

Packaging : Blister

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Norway

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06

SCI Medicinal Chemistry
Not Confirmed
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SCI Medicinal Chemistry
Not Confirmed

Nalmefene

Brand Name : Selincro

Dosage Form : Antic-calc Tablet, Film Coated

Dosage Strength : 18 mg

Packaging : Blister

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Norway

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07

SCI Medicinal Chemistry
Not Confirmed
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SCI Medicinal Chemistry
Not Confirmed

Nalmefene

Brand Name : Selincro

Dosage Form : Antic-calc Tablet, Film Coated

Dosage Strength : 18 mg

Packaging : Blister

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Norway

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08

SCI Medicinal Chemistry
Not Confirmed
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SCI Medicinal Chemistry
Not Confirmed

Nalmefenum

Brand Name : Selincro

Dosage Form : Filmtabl

Dosage Strength : 18mg

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Switzerland

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09

SCI Medicinal Chemistry
Not Confirmed
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SCI Medicinal Chemistry
Not Confirmed

Nalmefenum

Brand Name : Selincro

Dosage Form : Filmtabl

Dosage Strength : 18mg

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Switzerland

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10

SCI Medicinal Chemistry
Not Confirmed
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SCI Medicinal Chemistry
Not Confirmed

NALMEFENE HYDROCHLORIDE

Brand Name : REVEX

Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

Dosage Strength : EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1995-04-17

Application Number : 20459

Regulatory Info : DISCN

Registration Country : USA

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11

SCI Medicinal Chemistry
Not Confirmed
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SCI Medicinal Chemistry
Not Confirmed

NALMEFENE HYDROCHLORIDE

Brand Name : REVEX

Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

Dosage Strength : EQ 2MG BASE/2ML (EQ 1MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1995-04-17

Application Number : 20459

Regulatory Info : DISCN

Registration Country : USA

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12

SCI Medicinal Chemistry
Not Confirmed
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SCI Medicinal Chemistry
Not Confirmed

NALMEFENE HYDROCHLORIDE

Brand Name : OPVEE

Dosage Form : SPRAY;NASAL

Dosage Strength : EQ 2.7MG BASE/SPRAY

Packaging :

Approval Date : 2023-05-22

Application Number : 217470

Regulatory Info : RX

Registration Country : USA

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13

SCI Medicinal Chemistry
Not Confirmed
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SCI Medicinal Chemistry
Not Confirmed

NALMEFENE HYDROCHLORIDE

Brand Name : NALMEFENE HYDROCHLORIDE

Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

Dosage Strength : EQ 2MG BASE/2ML (EQ 1MG BASE/ML)

Packaging :

Approval Date : 2022-02-08

Application Number : 212955

Regulatory Info : RX

Registration Country : USA

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14

SCI Medicinal Chemistry
Not Confirmed
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SCI Medicinal Chemistry
Not Confirmed

NALMEFENE HYDROCHLORIDE

Brand Name : ZURNAI (AUTOINJECTOR)

Dosage Form : SOLUTION;INTRAMUSCULAR, SUBCUTANEOUS

Dosage Strength : EQ 1.5MG BASE/0.5ML (EQ 1.5MG BASE/0.5ML)

Packaging :

Approval Date : 2024-08-07

Application Number : 218590

Regulatory Info : DISCN

Registration Country : USA

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