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Last Updated: March 8, 2021

DrugPatentWatch Database Preview

Imipramine pamoate - Generic Drug Details

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What are the generic drug sources for imipramine pamoate and what is the scope of patent protection?

Imipramine pamoate is the generic ingredient in two branded drugs marketed by Hikma, Lupin Ltd, Mylan Pharms Inc, and Specgx Llc, and is included in four NDAs. Additional information is available in the individual branded drug profile pages.

There are thirty-four drug master file entries for imipramine pamoate. Two suppliers are listed for this compound.

Summary for imipramine pamoate
Drug Prices for imipramine pamoate

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Recent Clinical Trials for imipramine pamoate

Identify potential brand extensions & 505(b)(2) entrants

SponsorPhase
Shalvata Mental Health CenterN/A
Roxane LaboratoriesN/A

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Pharmacology for imipramine pamoate

US Patents and Regulatory Information for imipramine pamoate

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Mylan Pharms Inc IMIPRAMINE PAMOATE imipramine pamoate CAPSULE;ORAL 202338-003 Jun 28, 2013 DISCN No No   Start Trial   Start Trial   Start Trial
Lupin Ltd IMIPRAMINE PAMOATE imipramine pamoate CAPSULE;ORAL 090444-002 Apr 16, 2010 AB RX No No   Start Trial   Start Trial   Start Trial
Lupin Ltd IMIPRAMINE PAMOATE imipramine pamoate CAPSULE;ORAL 090444-001 Apr 16, 2010 AB RX No No   Start Trial   Start Trial   Start Trial
Lupin Ltd IMIPRAMINE PAMOATE imipramine pamoate CAPSULE;ORAL 090444-003 Apr 16, 2010 AB RX No No   Start Trial   Start Trial   Start Trial
Specgx Llc TOFRANIL-PM imipramine pamoate CAPSULE;ORAL 017090-001 Approved Prior to Jan 1, 1982 DISCN Yes No   Start Trial   Start Trial   Start Trial
Lupin Ltd IMIPRAMINE PAMOATE imipramine pamoate CAPSULE;ORAL 090444-004 Apr 16, 2010 AB RX No No   Start Trial   Start Trial   Start Trial
Hikma IMIPRAMINE PAMOATE imipramine pamoate CAPSULE;ORAL 091099-002 Apr 16, 2010 AB RX No No   Start Trial   Start Trial   Start Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

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