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Last Updated: March 29, 2024

MANNITOL 15% IN PLASTIC CONTAINER Drug Patent Profile


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When do Mannitol 15% In Plastic Container patents expire, and when can generic versions of Mannitol 15% In Plastic Container launch?

Mannitol 15% In Plastic Container is a drug marketed by B Braun and Icu Medical Inc and is included in two NDAs.

The generic ingredient in MANNITOL 15% IN PLASTIC CONTAINER is mannitol. There are eighteen drug master file entries for this compound. Nine suppliers are listed for this compound. Additional details are available on the mannitol profile page.

Drug patent expirations by year for MANNITOL 15% IN PLASTIC CONTAINER
Recent Clinical Trials for MANNITOL 15% IN PLASTIC CONTAINER

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

SponsorPhase
University Hospital Inselspital, BerneEarly Phase 1
Ecole Polytechnique Fédérale de LausanneEarly Phase 1
Centre Hospitalier Universitaire VaudoisEarly Phase 1

See all MANNITOL 15% IN PLASTIC CONTAINER clinical trials

Pharmacology for MANNITOL 15% IN PLASTIC CONTAINER
Drug ClassOsmotic Diuretic
Mechanism of ActionOsmotic Activity
Physiological EffectIncreased Diuresis

US Patents and Regulatory Information for MANNITOL 15% 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
B Braun MANNITOL 15% IN PLASTIC CONTAINER mannitol INJECTABLE;INJECTION 020006-003 Jul 26, 1993 AP RX No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Icu Medical Inc MANNITOL 15% IN PLASTIC CONTAINER mannitol INJECTABLE;INJECTION 019603-003 Jan 8, 1990 DISCN 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

EU/EMA Drug Approvals for MANNITOL 15% IN PLASTIC CONTAINER

Company Drugname Inn Product Number / Indication Status Generic Biosimilar Orphan Marketing Authorisation Marketing Refusal
Pharmaxis Europe Limited Bronchitol mannitol EMEA/H/C/001252
Bronchitol is indicated for the treatment of cystic fibrosis (CF) in adults aged 18 years and above as an add-on therapy to best standard of care.
Authorised no no no 2012-04-13
>Company >Drugname >Inn >Product Number / Indication >Status >Generic >Biosimilar >Orphan >Marketing Authorisation >Marketing Refusal

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