01/21/2026 | Press release | Distributed by Public on 01/21/2026 06:46
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Q4
|
Full Year
|
|||||||||||||||||||||||||||||||||||||
|
($ in Millions, except EPS)
|
2025
|
2024
|
% Change
|
2025
|
2024
|
% Change
|
||||||||||||||||||||||||||||||||
|
Reported Sales
|
|
$24,564
|
$22,520
|
9.1%
|
$94,193
|
$88,821
|
6.0%
|
|||||||||||||||||||||||||||||||
|
Net Earnings
|
$5,116
|
$3,431
|
49.1%
|
$26,804
|
$14,066
|
90.6%
|
||||||||||||||||||||||||||||||||
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EPS (diluted)
|
$2.10
|
$1.41
|
48.9%
|
$11.03
|
$5.79
|
90.5%
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||||||||||||||||||||||||||||||||
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|
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Q4
|
Full Year
|
||||||||||||||||||||||||||||||||||||
|
Non-GAAP* ($ in Millions, except EPS)
|
2025
|
2024
|
% Change
|
2025
|
2024
|
% Change
|
||||||||||||||||||||||||||||||||
|
Operational Sales1,2
|
|
|
7.1%
|
|
|
5.3%
|
||||||||||||||||||||||||||||||||
|
Adjusted Operational Sales1,3
|
|
|
6.1%
|
|
|
4.2%
|
||||||||||||||||||||||||||||||||
|
Adjusted Net Earnings1,4
|
$6,009
|
$4,946
|
21.5%
|
$26,215
|
$24,242
|
8.1%
|
||||||||||||||||||||||||||||||||
|
Adjusted EPS (diluted)1,4
|
$2.46
|
$2.04
|
20.6%
|
$10.79
|
$9.98
|
8.1%
|
||||||||||||||||||||||||||||||||
|
Free Cash Flow5,6
|
|
|
~$19,700
|
$19,842
|
|
|||||||||||||||||||||||||||||||||
|
Q4
|
|
|
|
% Change
|
|
|||||||||||||||
|
($ in Millions)
|
2025
|
2024
|
Reported
|
Operational1,2
|
Currency
|
Adjusted
Operational1,3
|
||||||||||||||
|
U.S.
|
$14,195
|
$13,204
|
7.5%
|
7.5
|
-
|
5.7
|
||||||||||||||
|
International
|
10,369
|
9,316
|
11.3
|
6.6
|
4.7
|
6.8
|
||||||||||||||
|
Worldwide
|
$24,564
|
$22,520
|
9.1%
|
7.1
|
2.0
|
6.1
|
||||||||||||||
|
|
|
|
|
|
|
|
||||||||||||||
|
Full Year
|
|
|
|
% Change
|
|
|||||||||||||||
|
($ in Millions)
|
2025
|
2024
|
Reported
|
Operational1,2
|
Currency
|
Adjusted
Operational1,3
|
||||||||||||||
|
U.S.
|
$53,752
|
$50,302
|
6.9%
|
6.9
|
-
|
4.9
|
||||||||||||||
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International
|
40,441
|
38,519
|
5.0
|
3.4
|
1.6
|
3.3
|
||||||||||||||
|
Worldwide
|
$94,193
|
$88,821
|
6.0%
|
5.3
|
0.7
|
4.2
|
||||||||||||||
|
Q4
|
|
|
|
% Change
|
|
|||||||||||||||
|
($ in Millions)
|
2025
|
2024
|
Reported
|
Operational1,2
|
Currency
|
Adjusted
Operational1,3
|
||||||||||||||
|
Innovative Medicine
|
$15,763
|
$14,332
|
10.0%
|
7.9
|
2.1
|
6.2
|
||||||||||||||
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MedTech
|
8,801
|
8,188
|
7.5
|
5.8
|
1.7
|
5.9
|
||||||||||||||
|
Worldwide
|
$24,564
|
$22,520
|
9.1%
|
7.1
|
2.0
|
6.1
|
||||||||||||||
|
Full Year
|
|
|
|
% Change
|
|
|||||||||||||||
|
($ in Millions)
|
2025
|
2024
|
Reported
|
Operational1,2
|
Currency
|
Adjusted
Operational1,3
|
||||||||||||||
|
Innovative Medicine
|
$60,401
|
$56,964
|
6.0%
|
5.3
|
0.7
|
4.1
|
||||||||||||||
|
MedTech
|
33,792
|
31,857
|
6.1
|
5.4
|
0.7
|
4.3
|
||||||||||||||
|
Worldwide
|
$94,193
|
$88,821
|
6.0%
|
5.3
|
0.7
|
4.2
|
||||||||||||||
|
($ in Billions, except EPS)
|
|
January 2026
|
||||||
|
Adjusted Operational Sales1,2
Change vs. Prior Year / Mid-point
|
|
5.4% - 6.4% / 5.9%
|
||||||
|
Operational Sales2 / Mid-point
Change vs. Prior Year / Mid-point
|
|
$99.5B - $100.5B / $100.0B
5.7% - 6.7% / 6.2%
|
||||||
|
Estimated Reported Sales3/ Mid-point
Change vs. Prior Year / Mid-point
|
|
$100.0B - $101.0B / $100.5B
6.2% - 7.2% / 6.7%
|
||||||
|
Adjusted Operational EPS (Diluted)2,4 / Mid-point
Change vs. Prior Year / Mid-point
|
|
$11.28 - $11.48 / $11.38
4.5% - 6.5% / 5.5%
|
||||||
|
Adjusted EPS (Diluted)3,4 / Mid-point
Change vs. Prior Year / Mid-point
|
|
$11.43 - $11.63 / $11.53
5.9% - 7.9% / 6.9%
|
||||||
| Regulatory |
Johnson & Johnson Submits OTTAVA Robotic Surgical System to the U.S. Food and Drug Administration1
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| Johnson & Johnson Receives FDA Approval for TRUFILL n-BCA Liquid Embolic System for the Treatment of Symptomatic Chronic Subdural Hematoma | |||||||||||
| U.S. FDA Approval of RYBREVANT FASPRO (amivantamab and hyaluronidase-lpuj) Enables the Simplest, Shortest Administration Time for a First-Line Combination Regimen when Combined with LAZCLUZE (lazertinib) | |||||||||||
| U.S. FDA approves AKEEGA as the first precision therapy for BRCA2-mutated metastatic castration-sensitive prostate cancer with 54% reduction in disease progression vs standard of care | |||||||||||
| DARZALEX FASPRO is the first and only treatment approved by the U.S. FDA for patients with high-risk smoldering multiple myeloma | |||||||||||
| FDA approval of CAPLYTA (lumateperone) has the potential to reset treatment expectations, offering hope for remission in adults with major depressive disorder | |||||||||||
| Data Releases |
New clinical data highlights CAPLYTA (lumateperone) as a promising option for achieving remission in adults with major depressive disorder1
|
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TECVAYLI monotherapy demonstrates superior progression-free and overall survival versus standard of care as early as first relapse in patients with multiple myeloma predominantly refractory to anti-CD38 therapy and lenalidomide1
|
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RYBREVANT (amivantamab-vmjw) longer-term results show promising and durable responses in difficult-to-treat colorectal cancer1
|
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Johnson & Johnson unveils new data showing nipocalimab is the first and only investigational FcRn blocker with potential to reduce systemic lupus erythematosus (SLE) activity in a Phase 2 study1
|
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| Unprecedented results from the Phase 3 MajesTEC-3 study support TECVAYLI plus DARZALEX FASPRO as a potential standard of care as early as second line for patients with relapsed/refractory multiple myeloma | |||||||||||
| Earlier use of CARVYKTI demonstrated lasting treatment-free remissions at 2.5 years in patients with relapsed or refractory multiple myeloma | |||||||||||
| Johnson & Johnson's INLEXZO (gemcitabine intravesical system) delivers 74 percent disease-free survival at one year in BCG-unresponsive, high-risk, papillary-only NMIBC | |||||||||||
| New long-term data reinforces TREMFYA (guselkumab) as the only IL-23 inhibitor proven to substantially inhibit structural joint damage in active psoriatic arthritis | |||||||||||
| Johnson & Johnson announces first head-to-head study comparing IMAAVY with an alternative FcRn blocker in generalized myasthenia gravis (gMG) at AANEM Annual Meeting | |||||||||||
| Icotrokinra maintains standout combination of therapeutic benefit and a favorable safety profile in once-daily pill through 28 weeks in ulcerative colitis | |||||||||||
| TREMFYA (guselkumab), the first and only IL-23 inhibitor with a fully subcutaneous treatment regimen, demonstrates durable remission in Crohn's disease at two years | |||||||||||
| Published in The Lancet: Nipocalimab significantly decreased Sjögren's disease (SjD) activity and severity through substantial reduction in Sjögren's-related autoantibodies | |||||||||||
| Icotrokinra long-term results affirm promise of targeted oral peptide with high rates of durable skin clearance and favorable safety profile in difficult-to-treat scalp and genital psoriasis | |||||||||||
| Subcutaneous amivantamab delivers promising 45 percent overall response rate with median duration of 7.2 months in recurrent or metastatic head and neck cancer | |||||||||||
| TECVAYLI plus DARZALEX FASPRO combination regimen significantly improves progression-free survival and overall survival versus standard of care | |||||||||||
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Other
|
Johnson & Johnson Reaches Agreement with U.S. Government to Improve Access to Medicines and Lower Costs for Millions of Americans; Delivers on U.S. Manufacturing and Innovation Investments1
|
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| Johnson & Johnson completes acquisition of Halda Therapeutics and its novel platform to revolutionize cancer treatment and enable next-generation oral therapies | |||||||||||
| Johnson & Johnson Announces Intent to Separate Its Orthopaedics Business | |||||||||||