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Jardiance vs Farxiga: label, access, and payer coverage compared

Jardiance (empagliflozin) and Farxiga (dapagliflozin) differ on outcomes data, generic status, and 2026 IRA pricing. Compare FDA labels, dosing, payer access, and step therapy.

Ran Chen
Ran Chen
11 min read · Published · Source-cited

Jardiance (empagliflozin, Boehringer Ingelheim/Eli Lilly) and Farxiga (dapagliflozin, AstraZeneca) are sodium-glucose cotransporter-2 (SGLT2) inhibitors that have evolved beyond type 2 diabetes into cornerstone therapies for heart failure and chronic kidney disease. Both have landmark outcome trial data, both are now on formulary for most plans, and both are subject to the IRA's Medicare Drug Price Negotiation Program starting in 2026.

But they are not identical in label scope, pivotal evidence, or payer positioning. This comparison is for prescribers, access teams, and pharmacists who need to understand the practical differences that affect coverage, step therapy, and prescribing decisions.

Short answer

Jardiance (empagliflozin)Farxiga (dapagliflozin)
Drug classSGLT2 inhibitorSGLT2 inhibitor
ManufacturerBoehringer Ingelheim / Eli LillyAstraZeneca
FDA indicationsT2D (age 10+), HF (HFrEF and HFpEF), CKD, CV death reduction in T2D + CVDT2D (age 10+), HF (HFrEF and HFpEF), CKD, HF hospitalization in T2D + CV risk
Generic availableNoYes (authorized generic dapagliflozin propanediol)
IRA negotiated price (2026)$197/month (30-day supply)$179/month (30-day supply)
Usual dosing10 mg once daily (HF/CKD/CV); 10 or 25 mg for T2D10 mg once daily (all indications)
Oral tabletYesYes
OTCNoNo
Prior authorizationVaries by plan; often required for CKD/HF without T2DVaries by plan; often required for CKD/HF without T2D
Step therapySome plans require Farxiga/generic dapagliflozin before JardianceSome plans require Jardiance before Farxiga (depending on formulary)

FDA-approved indications head-to-head

IndicationJardianceFarxiga
Glycemic control in T2D (age 10+)YesYes
CV death reduction in T2D + established CVDYes (EMPA-REG OUTCOME)Yes (DECLARE-TIMI 58)
Heart failure (reduced EF)Yes (EMPEROR-Reduced)Yes (DAPA-HF)
Heart failure (preserved EF)Yes (EMPEROR-Preserved)Yes (DELIVER)
CKD at risk of progressionYes (EMPA-KIDNEY)Yes (DAPA-CKD)
CKD without diabetesYesYes (first SGLT2i approved for CKD without diabetes)
HF hospitalization in T2D + CV riskYes (from EMPA-REG)Yes (DECLARE-TIMI 58)

Key label differences:

  • Farxiga was the first SGLT2 inhibitor specifically FDA-approved for CKD in patients without diabetes (based on DAPA-CKD, approved April 2021). Jardiance later gained the CKD indication with EMPA-KIDNEY.

  • Jardiance has a more established cardiovascular mortality signal (38% reduction in CV death in EMPA-REG OUTCOME), which was the primary driver of its cardiovascular indication.

  • Both are now recognized by ADA, AHA, ACC, and KDIGO guidelines as first-line options for patients with T2D and heart failure or CKD.

Pivotal trial evidence

Jardiance landmark trials

TrialPopulationPrimary endpointKey result
EMPA-REG OUTCOME7,020 adults with T2D + established CVD3-point MACE (CV death, non-fatal MI, non-fatal stroke)14% relative risk reduction; 38% reduction in CV death
EMPEROR-ReducedAdults with HFrEF (with or without T2D)CV death or HF hospitalization25% relative risk reduction
EMPEROR-PreservedAdults with HFpEF (with or without T2D)CV death or HF hospitalization21% relative risk reduction
EMPA-KIDNEY6,609 adults with CKD at risk of progressionKidney disease progression or CV death28% relative risk reduction

Farxiga landmark trials

TrialPopulationPrimary endpointKey result
DECLARE-TIMI 58Adults with T2D + established CVD or CV risk2-point MACE; HF hospitalization/CV deathNon-significant MACE reduction; significant 17% reduction in HF hospitalization/CV death
DAPA-HFAdults with HFrEF (with or without T2D)CV death or worsening HF26% relative risk reduction
DELIVERAdults with HFpEF (with or without T2D)CV death or worsening HF18% relative risk reduction
DAPA-CKDAdults with CKD (with or without T2D)Sustained eGFR decline, ESKD, renal/CV death39% relative risk reduction in composite kidney endpoint

The most notable difference: EMPA-REG OUTCOME demonstrated a stronger cardiovascular mortality signal for Jardiance (38% CV death reduction), while DAPA-CKD demonstrated a larger kidney-specific benefit for Farxiga (39% reduction in composite kidney endpoint in a broader CKD population including non-diabetic patients).

Dosing and administration

JardianceFarxiga
HF dose10 mg once daily10 mg once daily
CKD dose10 mg once daily10 mg once daily
T2D dose10 mg once daily; may increase to 25 mg5 mg or 10 mg once daily
T2D with CV disease dose10 mg once daily10 mg once daily
Renal impairment (T2D)Not recommended when eGFR <30 mL/min/1.73 m²Not recommended when eGFR <45 mL/min/1.73 m²
Renal impairment (HF/CKD)No dose adjustment for eGFR ≥20 mL/min/1.73 m²No dose adjustment for eGFR ≥25 mL/min/1.73 m²
With or without foodEitherEither
Available strengths10 mg, 25 mg tablets5 mg, 10 mg tablets

Both drugs carry the same class-level warnings: risk of diabetic ketoacidosis (even without markedly elevated blood glucose), acute kidney injury, serious urinary tract infections, genital mycotic infections, hypoglycemia when combined with insulin or sulfonylureas, and rare necrotizing fasciitis of the perineum (Fournier's gangrene).

Formulary and payer coverage

Commercial insurance

Both drugs are widely covered on commercial formularies, but step therapy direction varies by plan and PBM.

PBM/PayerJardianceFarxigaNotes
UnitedHealthcare commercial (2026 PDL)Tier 4; step therapy, quantity limitsStep therapy; quantity limits (generic dapagliflozin preferred)Generic dapagliflozin propanediol is listed at no cost-sharing as equivalent
OptumRx Premium Formulary (2026)Tier 2Tier 2 (Farxiga); generic dapagliflozin availableBoth preferred; generic dapagliflozin may have lower copay
Express Scripts National Preferred (2026)PreferredPreferred; generic dapagliflozin excluded from NPFBoth drugs preferred; counterintuitively, generic dapagliflozin is excluded from the NPF while brand Farxiga is preferred
CDPHP Medicare Part D (2026)Step therapy: requires trial of brand Farxiga firstPreferredSGLT2 step therapy group requires Farxiga trial before Jardiance
Kaiser Permanente (2026)CoveredCoveredCheck specific plan formulary

Step therapy patterns in 2026:

  • Some Medicare and commercial plans require a trial of Farxiga or generic dapagliflozin before approving Jardiance (e.g., CDPHP 2026 Medicare Part D step therapy list).

  • Other plans treat both as equivalent Tier 2 agents without step therapy requirements.

  • The availability of generic dapagliflozin is creating cost-based formulary preferences: where generic dapagliflozin is available at lower cost, plans may prefer it as the default SGLT2 inhibitor.

Medicare Part D (IRA-negotiated prices for 2026)

Both Jardiance and Farxiga were included in the first cycle of Medicare Drug Price Negotiation under the Inflation Reduction Act. The negotiated maximum fair prices (MFPs) became effective January 1, 2026:

DrugIRA-negotiated MFP (30-day supply)
Dapagliflozin (Farxiga)$179
Empagliflozin (Jardiance)$197.00

These represent significant reductions from prior list prices, which exceeded $600/month for both. Actual patient out-of-pocket costs depend on the plan's benefit design, coverage phase, and whether the patient qualifies for the Low-Income Subsidy (LIS):

  • Standard cost-sharing: 25% coinsurance during the initial coverage phase, up to the $2,100 annual out-of-pocket cap

  • LIS patients: $12.65 or less per fill

  • Medicare Prescription Payment Plan (MPPP): Monthly installments available instead of lump-sum cost-sharing

Generic dapagliflozin

Generic dapagliflozin propanediol (authorized generic of Farxiga) is now available. This is a significant development:

  • Generic dapagliflozin is priced lower than brand Farxiga and Jardiance

  • Some plans (e.g., UHC 2026 PDL) list generic dapagliflozin at no cost-sharing

  • The generic approval currently covers T2D and HF risk reduction indications; for the CKD indication, brand Farxiga remains the reference product

  • Jardiance does not yet have a generic equivalent

Medicaid

Both drugs are covered by state Medicaid programs, typically with minimal copay ($0–$8/month depending on state). Prior authorization may be required, particularly for non-T2D indications (HF without diabetes, CKD without diabetes).

Prior authorization considerations

When PA is typically required

  • HF or CKD indication without concurrent T2D diagnosis

  • Use in patients with eGFR below the label threshold

  • Dose escalation beyond standard dosing

  • Non-formulary or non-preferred SGLT2 inhibitor when step therapy applies

Required documentation

IndicationRequired documentation
T2D glycemic controlDiagnosis, current A1C, prior therapy records
Heart failureEchocardiogram or other EF assessment, NYHA class, BNP/NT-proBNP
CKDeGFR, urine albumin-to-creatinine ratio (uACR), CKD stage
CV risk reductionEstablished CVD documentation or CV risk factors

Switching between SGLT2 inhibitors

When formulary changes or access barriers require switching between Jardiance and Farxiga (or vice versa):

  • No washout period is required when switching within the SGLT2 inhibitor class

  • The patient can start the new drug at standard dosing immediately after stopping the previous one

  • For HF or CKD patients where treatment continuity is critical, avoid gaps longer than 3–5 days; consider a bridge supply or early refill if the switch is due to a formulary change rather than clinical failure

  • Document the reason for the switch (formulary mandate vs. clinical) in the PA submission, as payers may process formulary-driven switches more quickly

  • When switching from Farxiga to Jardiance for CKD, verify that the patient meets the Jardiance CKD label criteria (the patient populations in DAPA-CKD and EMPA-KIDNEY differ slightly)

Cost comparison

Cost metricJardianceFarxigaGeneric dapagliflozin
Average monthly cash price (no insurance)~$819 (30 tablets)~$776 (30 tablets)~$860 (30 tablets retail)
With discount coupon (SingleCare)~$255~$372~$207
IRA-negotiated Medicare price (2026)$197/month$179/monthLower than brand
Commercial copay with savings cardAs low as $0As low as $0N/A

Manufacturer savings programs

DrugProgramBenefit
JardianceJardiance Savings Card (commercially insured)As low as $0 per fill; annual maximum applies
FarxigaFarxiga Savings Card (commercially insured)As low as $0 per fill
JardianceMedicare Resource GuideInformation on cost support options for Part D patients
FarxigaAstraZeneca patient assistanceSupport for qualifying uninsured or underinsured patients

What changed in 2026

  • IRA-negotiated Medicare prices in effect: Both Jardiance ($197/month) and Farxiga ($179/month) now have government-negotiated prices under the Inflation Reduction Act, reducing costs significantly for Medicare beneficiaries.

  • Generic dapagliflozin availability: The authorized generic of Farxiga is now on market, creating a cost advantage for some plans and formularies.

  • Step therapy divergence: Some Medicare Part D plans (e.g., CDPHP) require Farxiga trial before covering Jardiance, while others treat both as equivalent. The availability of generic dapagliflozin is driving formulary decisions.

  • Updated clinical guidelines: ADA 2026 Standards of Care and KDIGO 2024 CKD guidelines both recommend SGLT2 inhibitors as first-line therapy for patients with T2D and heart failure or CKD, regardless of A1C level.

  • EMPA-KIDNEY publication impact: Jardiance's CKD indication is now well-established, narrowing the previous gap where Farxiga had a clearer CKD label advantage.

What to monitor

  • Generic dapagliflozin label expansion: Whether the FDA expands generic dapagliflozin labeling to include the CKD indication (currently only brand Farxiga carries the full CKD label).

  • Formulary shifts driven by generic pricing: As generic dapagliflozin costs decrease, expect more plans to prefer it over both brand Farxiga and Jardiance.

  • IRA negotiation cycle 2: Monitor whether either drug is re-negotiated or whether pricing changes in future years.

  • Jardiance generic entry timeline: Monitor when empagliflozin exclusivity ends, which could equalize the cost landscape.

  • New SGLT2 competitors: Monitor any new SGLT2 inhibitor approvals or label expansions (e.g., Inpefa/sotagliflozin) that could shift formulary positioning.

  • CKD guideline updates: KDIGO and ADA may issue refined guidance on SGLT2 inhibitor selection based on patient-specific factors (eGFR range, albuminuria severity, heart failure type).

Sources

Ran Chen
Contributing Editor
Ran Chen

Founder, PharmaDossier. Life-sciences operator covering market access, specialty pharma, biosimilars, and regulated healthcare growth.

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