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01 2Amdipharm Mercury Company Limited
02 2Amdipharm Mercury Debtco Limited
03 4Hikma Pharmaceuticals
04 4Lupin Ltd
05 4Mallinckrodt Pharmaceuticals
06 1Montage Laboratories
07 3Neuraxpharm
08 2Pharmaco Distribution
09 1Pro Pharmaceuticals Group Pty. Ltd.
10 4Rising Pharmaceuticals Inc
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01 16CAPSULE;ORAL
02 3Film Coated Tablet
03 1Imipramine 10Mg 60 Units Oral Use
04 1Imipramine 25Mg 50 Combined Oral Use
05 1Liquid Injection
06 2TAB
07 2tablet
08 1Blank
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01 8DISCN
02 2Originator
03 8RX
04 9Blank
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01 12IMIPRAMINE PAMOATE
02 1Imipramine
03 1Imipramine (Leading)
04 4TOFRANIL-PM
05 4Tofranil
06 1Tofranil 10
07 1Tofranil 25
08 3Blank
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01 3Australia
02 1India
03 2Italy
04 2South Africa
05 3Spain
06 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 : 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 : 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