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What's Happening

Stay up to date on conferences, social posts, and what’s new with Healthesystems

Events

Let’s connect at one of our upcoming conferences or speaking engagements
August 17 - Aug 20, 2025

WCI

Healthesystems is attending and exhibiting at the Workers’ Compensation Institute conference, which brings together workers’ compensation professionals.

Orlando, FL
September 07 - Sep 11, 2025

STRIMA Annual Conference

Healthesystems is attending the State Risk & Insurance Management Association Annual Conference, which brings together risk and insurance managers of state governments.

Jekyll Island, GA
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MedMonitor

An up-to-date timeline of FDA approvals that could impact workers' comp
View All MedMonitor Information

Janumet® XR (sitagliptin phosphate and metformin hydrochloride) extended-release tablets

Approval Date: Jun 2025

Note: First-Time Generic

Indicated as an adjunct to diet and exercise to improve glycemic control for the treatment of type 2 diabetes

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Xarelto® XR (rivaroxaban) extended-release tablets

Approval Date: Jun 2025

Note: First-Time Generic

Indicated to reduce the risk of stroke, major cardiovascular events in patients with coronary artery disease, and for the treatment of several other cardiovascular concerns

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Xarelto® (rivaroxaban) tablets

Approval Date: May 2025

Note: First-Time Generic

Indicated to reduce the risk of stroke, major cardiovascular events in patients with coronary artery disease, and for the treatment of several other cardiovascular concerns. In March, a 2.5 mg dose of this generic was approved; this approval applies to 10 mg, 15 mg, and 20 mg doses

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Fycompa® (perampanel) tablets

Approval Date: May 2025

Note: First-Time Generic

Indicated as an adjunctive therapy for the treatment of partial-onset seizures with or without secondarily generalized seizures, and primary generalized tonic-clonic seizures in patients with epilepsy.

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Brekiya® (dihydroergotamine mesylate) injection

Approval Date: May 2025

Note: New Product/New Formulation

While DHE has been available since 1946, this is the first DHE drug available in a ready-to-use autoinjector, indicated for the acute treatment of migraine with or without aura and the acute treatment of cluster headaches

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Yutrepia™ (treprostinil) inhalation powder

Approval Date: May 2025

Note: New Product/New Formulation

Indicated for the treatment of pulmonary arterial hypertension, this is the first and only dry-powder formulation of treprostinil

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Starjemza (Ustekinumab-hmny) injection

Approval Date: May 2025

Note: Biosimilar

A biosimilar to Stelara (ustekinumab), this drug is indicated for the treatment of moderate to severe plaque psoriasis, active psoriatic arthritis, moderate to severely active Crohn’s disease, and moderate to severely active Ulcerative Colitis

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Atzumi™ (dihydroergotamine (DHE)) nasal powder

Approval Date: Apr 2025

Note: New Product/New Formulation

While DHE has been available since 1946, this is the first DHE drug available in a nasal powder formulation and indicated for the acute treatment of migraine with or without aura

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Arbli (losartan potassium) oral suspension

Approval Date: Mar 2025

Note: New Product

Indicated for the treatment of hypertension, stroke risk reduction in patients with hypertension and left ventricular hypertrophy, and diabetic neuropathy in certain type 2 diabetes patients with hypertension

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Tyenne® (tocilizumab-aazg) injection

Approval Date: Mar 2025

Note: New Indication

A biosimilar to Acterma®, this autoimmune drug has received an additional indication for the treatment of COVID-19 in hospitalized patients who are receiving systemic corticosteroids and require supplemental oxygen, non-invasive or invasive mechanical ventilation, or extracorporeal membrane oxygenation (ECMO)

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Symbravo® (meloxicam and rizatriptan) tablets

Approval Date: Jan 2025

Note: New Product

A combination NSAID and triptan drug indicated for the acute treatment of migraine with or without aura

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Spravato® (esketamine) nasal spray, CIII

Approval Date: Jan 2025

Note: New Indication

An NMDA receptor antagonist, this drug is now indicated for use as a monotherapy for treatment-resistant depression (TRD). Spravato originally required conjunctive use with an oral antidepressant for (TRD)

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Avtozma® (tocilizumab-anoh) injection

Approval Date: Jan 2025

Note: Biosimilar

A biosimilar to Acterma, this drug is indicated for the treatment of rheumatoid arthritis, giant cell arthritis, and COVID-19 in hospitalized patients receiving supplemental oxygen and corticosteroids

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Journavx (suzetrigine) tablets

Approval Date: Jan 2025

Note: New Product

A novel, first-in-class, non-opioid analgesic indicated for the treatment of moderate to severe acute pain. Journavx targets pain-signaling pathways involving sodium channels and has not been studied for use beyond 14 days

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Victoza® (liraglutide) injection

Approval Date: Dec 2024

Note: First-Time Generic

A GLP-1 receptor agonist, this first-time generic is indicated for the once-daily treatment of type 2 diabetes, in conjunction with diet and exercise

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