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01 8Novartis Pharmaceuticals Corporation
02 4RELIANCE FORMULATION PVT. LTD
03 2XL Laboratories Private Limited
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01 4Film Coated Tablet
02 1Oral Drops
03 2SUSPENSION;ORAL
04 2TABLET
05 5Tablet
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01 2DISCN
02 6Deregistered
03 2Generic
04 4Blank
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01 2MELLARIL-S
02 5Mallorol
03 1Mallorol Retard
04 1RIDAZ
05 1RIDAZ-100
06 1ZENERIL -10 TABS
07 1ZENERIL -25 TAB
08 1ZENERIL -50 TAB
09 1ZENERIL PLUS - H
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01 6India
02 6Sweden
03 2USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : MELLARIL-S
Dosage Form : SUSPENSION;ORAL
Dosage Strength : EQ 25MG HYDROCHLORIDE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 17923
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : MELLARIL-S
Dosage Form : SUSPENSION;ORAL
Dosage Strength : EQ 100MG HYDROCHLORIDE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 17923
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Mallorol
Dosage Form : Film Coated Tablet
Dosage Strength : 10mg
Packaging :
Approval Date : 28/06/1960
Application Number : 19600628000031
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Mallorol
Dosage Form : Film Coated Tablet
Dosage Strength : 100mg
Packaging :
Approval Date : 28/06/1960
Application Number : 19600628000055
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Mallorol
Dosage Form : Film Coated Tablet
Dosage Strength : 25mg
Packaging :
Approval Date : 28/06/1960
Application Number : 19600628000048
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Mallorol
Dosage Form : Oral Drops
Dosage Strength : 30mg/ml
Packaging :
Approval Date : 19/10/1961
Application Number : 19611019000011
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Mallorol
Dosage Form : Film Coated Tablet
Dosage Strength : 50mg
Packaging :
Approval Date : 15/11/1961
Application Number : 19611115000014
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Mallorol Retard
Dosage Form : Tablet
Dosage Strength : 200mg
Packaging :
Approval Date : 16/08/1968
Application Number : 19680816000012
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info :
Registration Country : India
Brand Name : ZENERIL -10 TABS
Dosage Form : Tablet
Dosage Strength : 10MG
Packaging :
Approval Date :
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Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name : ZENERIL -25 TAB
Dosage Form : Tablet
Dosage Strength : 25MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name : ZENERIL -50 TAB
Dosage Form : Tablet
Dosage Strength : 50MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Thioridazine; Trifluoperazine hydrochoride; Trihexyphenidyl
Brand Name : ZENERIL PLUS - H
Dosage Form : Tablet
Dosage Strength : 25MG; 5MG; 2MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : Generic
Registration Country : India
Brand Name : RIDAZ-100
Dosage Form : TABLET
Dosage Strength : 50MG
Packaging :
Approval Date :
Application Number : 88004
Regulatory Info : Generic
Registration Country : India
Regulatory Info : Generic
Registration Country : India
Brand Name : RIDAZ
Dosage Form : TABLET
Dosage Strength : 100MG
Packaging :
Approval Date :
Application Number : 88004
Regulatory Info : Generic
Registration Country : India