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01 6H. Lundbeck AS
02 2Hikma Pharmaceuticals
03 1Indivior
04 2Purdue Pharmaceuticals L.P
05 3Sichuan Qingmu Pharmaceutical
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01 3Antic-calc Tablet, Film Coated
02 1FILM COATED PILL
03 2Filmtabl
04 6SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
05 1SOLUTION;INTRAMUSCULAR, SUBCUTANEOUS
06 1SPRAY;NASAL
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01 2DISCN
02 5RX
03 7Blank
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01 4NALMEFENE HYDROCHLORIDE
02 1OPVEE
03 2REVEX
04 6Selincro
05 1ZURNAI (AUTOINJECTOR)
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01 3Norway
02 1Sweden
03 2Switzerland
04 8USA
Regulatory Info :
Registration Country : Sweden
Brand Name : Selincro
Dosage Form : FILM COATED PILL
Dosage Strength : 18 MG
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Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Norway
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
Regulatory Info :
Registration Country : Norway
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
Regulatory Info :
Registration Country : Norway
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
Regulatory Info :
Registration Country : Switzerland
Brand Name : Selincro
Dosage Form : Filmtabl
Dosage Strength : 18mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Switzerland
Brand Name : Selincro
Dosage Form : Filmtabl
Dosage Strength : 18mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info : DISCN
Registration Country : USA
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Strength : EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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 : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info :
Registration Country : USA
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