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Liquidia Submits Amendment to Add PH-ILD Indication to Tentatively Approved NDA for YUTREPIA™ (treprostinil) Inhalation Powder

No new clinical data is required to add PH-ILD indication as per FDA correspondenceRecertified that YUTREPIA does not infringe any valid patents listed in the Orange Book for TyvasoPreparing for.

United statesRoger jeffsJason adairUs district courtYork heart associationUnited therapeutics corporationDrug administrationLiquidia technologies incLiquidia corporationOrange bookNapproved drug productsTherapeutic equivalence evaluationsUnited therapeuticsPatent trialAppeal boardChief executive officer

Liquidia Technologies (LQDA) Submits Amendment to Add PH-ILD Indication to Tentatively Approved NDA for YUTREPIA

Liquidia Technologies (LQDA) Submits Amendment to Add PH-ILD Indication to Tentatively Approved NDA for YUTREPIA
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United statesRoger jeffsLiquidia corporationDrug administrationLiquidia technologies incUnited therapeutics corporationUs district courtYork heart associationNapproved drug productsTherapeutic equivalence evaluationsOrange bookUnited therapeuticsPatent trialAppeal boardChief executive officerNew york heart association

Form 424B5 NeuBase Therapeutics,

Form 424B5 NeuBase Therapeutics,
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By Leaving Therapeutic Alternatives Undefined, CMS Tilts The Playing Field Of Drug Price Negotiations

By Leaving Therapeutic Alternatives Undefined, CMS Tilts The Playing Field Of Drug Price Negotiations
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Previewing Generic s Skinny Label: Supreme Court to Rule on Teva s Certiorari Petition | Foley Hoag LLP

The Supreme Court is expected to consider Teva’s pending petition for certiorari in the highly anticipated GlaxoSmithKline LLC v. Teva Pharms. USA, Inc. on May 11, 2023, a case that.

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