01 2Amdipharm Mercury Company Limited
02 2Amdipharm Mercury Debtco Limited
03 4Hikma Pharmaceuticals
04 4Lupin Ltd
05 4Mallinckrodt Pharmaceuticals
06 3Neuraxpharm
07 2Pharmaco Distribution
08 1Pro Pharmaceuticals Group Pty. Ltd.
09 4Rising Pharmaceuticals Inc
01 16CAPSULE;ORAL
02 3Film Coated Tablet
03 1Imipramine 10Mg 60 Units Oral Use
04 1Imipramine 25Mg 50 Combined Oral Use
05 2TAB
06 2tablet
07 1Blank
01 8DISCN
02 2Originator
03 8RX
04 8Blank
01 12IMIPRAMINE PAMOATE
02 1Imipramine (Leading)
03 4TOFRANIL-PM
04 4Tofranil
05 1Tofranil 10
06 1Tofranil 25
07 3Blank
01 3Australia
02 2Italy
03 2South Africa
04 3Spain
05 16USA
Regulatory Info :
Registration Country : Italy
Brand Name : Tofranil
Dosage Form : Imipramine 10Mg 60 Units Oral Use
Dosage Strength : 60 cpr riv 10 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Tofranil
Dosage Form : Imipramine 25Mg 50 Combined Oral Use
Dosage Strength : 50 cpr riv 25 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Australia
Brand Name : Tofranil 10
Dosage Form : tablet
Dosage Strength : 10 mg
Packaging : 50
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Brand Name : Tofranil 25
Dosage Form : tablet
Dosage Strength : 25 mg
Packaging : 50
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info : RX
Registration Country : USA
Brand Name : IMIPRAMINE PAMOATE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 75MG HYDROCHLORIDE
Packaging :
Approval Date : 2010-04-16
Application Number : 91099
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : IMIPRAMINE PAMOATE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 100MG HYDROCHLORIDE
Packaging :
Approval Date : 2010-04-16
Application Number : 91099
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : IMIPRAMINE PAMOATE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 125MG HYDROCHLORIDE
Packaging :
Approval Date : 2010-04-16
Application Number : 91099
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : IMIPRAMINE PAMOATE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 150MG HYDROCHLORIDE
Packaging :
Approval Date : 2010-04-16
Application Number : 91099
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : IMIPRAMINE PAMOATE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 75MG HYDROCHLORIDE
Packaging :
Approval Date : 2010-04-16
Application Number : 90444
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : IMIPRAMINE PAMOATE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 100MG HYDROCHLORIDE
Packaging :
Approval Date : 2010-04-16
Application Number : 90444
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : IMIPRAMINE PAMOATE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 125MG HYDROCHLORIDE
Packaging :
Approval Date : 2010-04-16
Application Number : 90444
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : IMIPRAMINE PAMOATE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 150MG HYDROCHLORIDE
Packaging :
Approval Date : 2010-04-16
Application Number : 90444
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TOFRANIL-PM
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 75MG HYDROCHLORIDE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 17090
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TOFRANIL-PM
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 150MG HYDROCHLORIDE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 17090
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TOFRANIL-PM
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 125MG HYDROCHLORIDE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 17090
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TOFRANIL-PM
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 100MG HYDROCHLORIDE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 17090
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : Spain
Brand Name :
Dosage Form : Film Coated Tablet
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Spain
Regulatory Info :
Registration Country : Spain
Brand Name :
Dosage Form : Film Coated Tablet
Dosage Strength : 25MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Spain
Regulatory Info :
Registration Country : Spain
Brand Name :
Dosage Form : Film Coated Tablet
Dosage Strength : 100MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Spain
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Tofranil
Dosage Form : TAB
Dosage Strength : 10mg
Packaging : 100X1mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Tofranil
Dosage Form : TAB
Dosage Strength : 25mg
Packaging : 100X1mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : DISCN
Registration Country : USA
Brand Name : IMIPRAMINE PAMOATE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 75MG HYDROCHLORIDE
Packaging :
Approval Date : 2013-06-28
Application Number : 202338
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : IMIPRAMINE PAMOATE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 100MG HYDROCHLORIDE
Packaging :
Approval Date : 2013-06-28
Application Number : 202338
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : IMIPRAMINE PAMOATE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 125MG HYDROCHLORIDE
Packaging :
Approval Date : 2013-06-28
Application Number : 202338
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : IMIPRAMINE PAMOATE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 150MG HYDROCHLORIDE
Packaging :
Approval Date : 2013-06-28
Application Number : 202338
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : Australia
Brand Name : Imipramine (Leading)
Dosage Form :
Dosage Strength :
Packaging : 100
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
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