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Last Updated: April 19, 2024

MILRINONE LACTATE IN PLASTIC CONTAINER Drug Patent Profile


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When do Milrinone Lactate In Plastic Container patents expire, and what generic alternatives are available?

Milrinone Lactate In Plastic Container is a drug marketed by Hikma Farmaceutica and is included in one NDA.

The generic ingredient in MILRINONE LACTATE IN PLASTIC CONTAINER is milrinone lactate. There are nine drug master file entries for this compound. Thirteen suppliers are listed for this compound. Additional details are available on the milrinone lactate profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Milrinone Lactate In Plastic Container

A generic version of MILRINONE LACTATE IN PLASTIC CONTAINER was approved as milrinone lactate by FRESENIUS KABI USA on May 28th, 2002.

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Summary for MILRINONE LACTATE IN PLASTIC CONTAINER
Drug patent expirations by year for MILRINONE LACTATE IN PLASTIC CONTAINER
Recent Clinical Trials for MILRINONE LACTATE IN PLASTIC CONTAINER

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

SponsorPhase
Shanghai Children's Medical CenterPhase 3
Ottawa Heart Institute Research CorporationPhase 4
University of PennsylvaniaN/A

See all MILRINONE LACTATE IN PLASTIC CONTAINER clinical trials

Pharmacology for MILRINONE LACTATE IN PLASTIC CONTAINER
Anatomical Therapeutic Chemical (ATC) Classes for MILRINONE LACTATE IN PLASTIC CONTAINER

US Patents and Regulatory Information for MILRINONE LACTATE IN PLASTIC CONTAINER

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Hikma Farmaceutica MILRINONE LACTATE IN PLASTIC CONTAINER milrinone lactate INJECTABLE;INJECTION 090038-001 Jan 21, 2010 AP RX No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Hikma Farmaceutica MILRINONE LACTATE IN PLASTIC CONTAINER milrinone lactate INJECTABLE;INJECTION 090038-002 Jan 21, 2010 AP RX No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a 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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