JNJ

Johnson & Johnson
NYSEHEALTHCAREDRUG MANUFACTURERS - GENERAL

Key Statistics

Market Cap
$653.61B
P/E Ratio
31.46
EPS
$8.62
Beta
0.23
52W High
$281.07
52W Low
$177.06
50-Day MA
$264.54
200-Day MA
$239.98
Dividend Yield
1.94%
Profit Margin
21.50%
Forward P/E
21.01
PEG Ratio
2.82

About Johnson & Johnson

Johnson & Johnson (J&J) is an American multinational corporation founded in 1886 that develops medical devices, pharmaceuticals, and consumer packaged goods. Its common stock is a component of the Dow Jones Industrial Average and the company is ranked No. 36 on the 2021 Fortune 500 list of the largest United States corporations by total revenue. Johnson & Johnson is one of the world's most valuable companies, and is one of only two U.S.-based companies that has a prime credit rating of AAA, higher than that of the United States government.

Official WebsiteUSAFY End: December

Fundamentals

Revenue (TTM)$97.93B
Gross Profit (TTM)$66.73B
EBITDA$34.87B
Operating Margin29.20%
Return on Equity25.70%
Return on Assets8.60%
Revenue/Share (TTM)$40.67
Book Value$35.28
Price-to-Book7.63
Price-to-Sales (TTM)6.67
EV/Revenue6.91
EV/EBITDA19.94
Quarterly Earnings Growth (YoY)-0.90%
Quarterly Revenue Growth (YoY)6.60%
Shares Outstanding$2.41B
Float$2.41B
% Insiders0.05%
% Institutions76.72%

Historical Volatility

HV 10-Day
6.15%
HV 20-Day
15.27%
HV 30-Day
18.89%
HV 60-Day
22.04%
HV Rank
64.7%

Volatility is currently contracting

Analyst Ratings

Consensus ($277.91 target)
5
Strong Buy
11
Buy
6
Hold
1
Sell

Latest News

Johnson & Johnson's Next Growth Engine Is Taking Shape

Johnson & Johnson's oncology and immunology pipeline is firing on multiple cylinders, but a collapsing blockbuster drug and mounting litigation costs threaten to cancel out every gain. Here is whether the bull case or the headwinds win.

24/7 Wall Street9/28/2026Positive
Johnson & Johnson says Tremfya eases spinal pain in Phase 4 psoriatic arthritis study

Johnson & Johnson (NYSE:JNJ) said its Tremfya treatment significantly improved spinal pain and stiffness in adults with axial psoriatic arthritis in a Phase 4 study. The company said Tremfya met the study's primary endpoint at week 24, showing greater improvement than placebo on a disease activity measure that includes spinal pain and stiffness.

Proactive Investors9/25/2026Positive
Johnson & Johnson announces TREMFYA® (guselkumab) is the first and only IL-23 inhibitor to show significant improvement in spinal pain and stiffness in landmark axial psoriatic arthritis (PsA) study

Topline results show TREMFYA met the primary and major secondary endpoints of axial involvement in PsA - including spinal pain and stiffness - and demonstrated significant improvement in MRI-confirmed inflammation First-ever study to use objective MRI assessments to confirm presence of axial involvement and demonstrate axial inflammation reduction in PsA SPRING HOUSE, Pa., Sept. 25, 2026 /PRNewswire/ -- Johnson & Johnson (NYSE: JNJ) today announced that TREMFYA® (guselkumab) met the primary and major secondary endpoints demonstrating both improvement in axial symptoms and reduction in inflammation by MRI assessment in the Phase 4 STAR study evaluating biologic-naïve adults with active psoriatic arthritis and axial involvement (axial PsA).

PRNewsWire9/25/2026Neutral
Single infusion of CARVYKTI® (ciltacabtagene autoleucel) delivered five-year treatment-free remissions in 50% of patients in early line relapsed/refractory multiple myeloma

New results suggest earlier treatment may increase the likelihood of long-term remission Study adds  to Johnson & Johnson's overwhelming body of evidence supporting its innovative multiple myeloma therapies in second line, where earlier intervention may increase long-term remission and disease control RARITAN, N.J., Sept. 25, 2026 /PRNewswire/ -- Johnson & Johnson (NYSE:JNJ), a worldwide leader in multiple myeloma therapies, announced today new long-term follow-up data from the initial subgroup of cohort A in the Phase 2 CARTITUDE-2 study (N=20) showing that 50% of patients (10/20) in early line relapsed or refractory multiple myeloma (RRMM) who were treated with a single infusion of CARVYKTI® (ciltacabtagene autoleucel; cilta-cel) remained alive and progression-free for at least five years without maintenance therapy.1 These results build on the durable, treatment-free remissions observed in the CARTITUDE-1 study, which evaluated patients in later lines of therapy, and reinforce that earlier treatment with CARVYKTI® may increase long-term remission and disease control.

PRNewsWire9/25/2026Neutral
2026 2H Healthcare Dividend Roundup: Johnson & Johnson Outshines AbbVie

Johnson & Johnson trades at a 30% P/E premium to AbbVie (24.2x vs. 18.8x on FY1 basis). The premium is further amplified on a PEGY basis (4.80x vs. 2.33x) when yield and growth are factored in. However, JNJ's premium is well justified by its conservative balance sheet and superior capital allocation flexibility.

Seeking Alpha9/23/2026Positive
New model-based analysis further supports the potential of TECVAYLI® (teclistamab-cqyv) plus DARZALEX FASPRO® (daratumumab and hyaluronidase-fihj) to redefine long-term survival expectations in early line relapsed/refractory multiple myeloma

Analysis shows ~87% of patients treated with TECVAYLI® plus DARZALEX FASPRO® as early as second line were estimated to have comparable mortality risk to the general population A separate analysis shows the survival benefit was driven by a 90% reduction in the risk of multiple myeloma progression versus standard of care, with no significant difference in rates of non-relapse mortality  Johnson & Johnson is advancing a differentiated multiple myeloma portfolio designed to deliver deeper, more durable disease control and improve long-term outcomes for patients  RARITAN, N.J., Sept. 23, 2026 /PRNewswire/ -- Johnson & Johnson (NYSE:JNJ), a worldwide leader in multiple myeloma therapies, today announced new data from the Phase 3 MajesTEC-3 study showing sustained disease control and survival with TECVAYLI® (teclistamab-cqyv) plus DARZALEX FASPRO® (daratumumab and hyaluronidase-fihj) in patients with relapsed or refractory multiple myeloma (RRMM) who had received 1-3 prior lines of therapy.1,2 Using a relative survival mixture cure model (MCM) and actual progression-free survival (PFS) and overall survival (OS) data from the trial, statistical modeling estimated that ~87% of patients treated with TECVAYLI® plus DARZALEX FASPRO ®  (Tec-Dara) may experience a mortality risk and projected life expectancy similar to an age-matched general population.1 Modeling further predicted that median overall survival with Tec-Dara would be nearly four-fold longer than with the standard of care (SOC) comparator in the study, dexamethasone with pomalidomide or bortezomib (DPd/DVd).

PRNewsWire9/23/2026Neutral

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Data last updated: 9/28/2026