Johnson & Johnson (BIT:1JNJ)
Italy · Delayed Price · Currency is EUR | Market Cap | 502.70B +39.8% |
| Revenue (ttm) | 80.06B +6.0% |
| Net Income | 22.78B +90.6% |
| EPS | 9.38 +90.5% |
| Shares Out | n/a |
| PE Ratio | 22.06 |
| Forward PE | 20.62 |
| Dividend | 3.39 (1.62%) |
| Ex-Dividend Date | Nov 24, 2025 |
| Volume | 241 |
| Average Volume | 127 |
| Open | 208.50 |
| Previous Close | 208.75 |
| Day's Range | 206.15 - 209.60 |
| 52-Week Range | 127.72 - 234.20 |
| Beta | n/a |
| RSI | 55.75 |
| Earnings Date | Apr 14, 2026 |
About Johnson & Johnson
Johnson & Johnson, together with its subsidiaries, engages in the research and development, manufacture, and sale of a range of products in the healthcare field worldwide. It operates in two segments, Innovative Medicine and MedTech. The Innovative Medicine segment offers products for various therapeutic areas, such as oncology, immunology, neuroscience, pulmonary hypertension, infectious diseases, and cardiovascular and metabolism distributed through retailers, wholesalers, distributors, hospitals, and healthcare professionals for prescription... [Read more]
Financial Performance
In 2025, Johnson & Johnson's revenue was $94.19 billion, an increase of 6.05% compared to the previous year's $88.82 billion. Earnings were $26.80 billion, an increase of 90.56%.
Financial numbers in USD Financial StatementsNews
Johnson & Johnson (JNJ) Price Forecast: Bull Flag Signals Strength
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Johnson & Johnson's DARZALEX® (daratumumab) becomes the first oncology injectable approved for administration by patients or caregivers
Landmark decision by CHMP grants approval for self or caregiver administration for patients living with multiple myeloma1 Milestone is a testament to ten years of daratumumab experience and innovation...
Johnson & Johnson: Deserves A Place In Conservative Dividend Growth Portfolios
Johnson & Johnson demonstrates a robust historical dividend growth profile, highlighted by 63 years of consecutive hikes. JNJ has an AAA credit rating, adding safety for the dividend. Though there are...
Protagonist Partners With Johnson & Johnson To Compete With AbbVie's Skyrizi
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Best Dividend Aristocrats As Of March 20, 2026
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The Big 3: ORCL, JNJ, SBUX
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JNJ Stock's Re-Rating: When The Market Finally Sees A Different Company
Question: What caused JNJ stock to rise 70% since early 2025?
TrumpRx lists many medicines at prices higher than paid in UK
U.S. President Donald Trump pledged to make prescription drugs cheaper for Americans than anywhere in the world, but his TrumpRx.gov website is not delivering across the board lower prices than those ...
FDA approves psoriasis pill from J&J that rivals shots Tremfya, Skyrizi
Johnson & Johnson said the FDA has approved its once-daily psoriasis pill Icotyde. Icotyde targets IL-23, rivaling best-selling shots Tremfya and Skyrizi.
US FDA approves J&J's oral psoriasis pill
The U.S. Food and Drug Administration has approved Johnson & Johnson's oral pill for psoriasis, the company said on Wednesday, paving the way for a more convenient treatment option for patients with...
FDA approval of ICOTYDE™ (icotrokinra) ushers in new era for first-line systemic treatment of plaque psoriasis with a targeted oral peptide
Johnson & Johnson introduces the first and only IL-23R targeted oral peptide that delivers complete skin clearance and favorable safety profile in a once-daily pill ICOTYDE offers an innovative new op...
Johnson & Johnson Drives Innovation in Pulsed Field Ablation with Peru Launch
LIMA, Peru--(BUSINESS WIRE)--Johnson & Johnson announced the arrival in Peru of a new pulsed field ablation (PFA) technology for the treatment of drug-refractory paroxysmal atrial fibrillation. This i...
Johnson & Johnson highlights promising first-in-human Erda-iDRS (formerly TAR-210) results in intermediate-risk non-muscle-invasive bladder cancer
Data presented at EAU 2026 show an 89 percent complete response rate in intermediate-risk disease with durable responses observed over 18 months and tolerable safety profile Erda-iDRS has the potenti...
Johnson & Johnson Announces FDA Approval of TECNIS PureSee Intraocular Lens, a Breakthrough Solution for U.S. Cataract Patients
JACKSONVILLE, Fla.--(BUSINESS WIRE)--Johnson & Johnson Announces FDA Approval of TECNIS PureSee Intraocular Lens, a Breakthrough Solution for U.S. Cataract Patients.
Goldman Sachs Large Cap Equity Fund Q4 2025 Portfolio Activity
Our position in American pharmaceutical company, Eli Lilly & Company (1.8%), was a top contributor to relative returns during the fourth quarter. Our position in global semiconductor company, Advanced...
Johnson & Johnson (JNJ) Presents at Barclays 28th Annual Global Healthcare Conference Transcript
Johnson & Johnson (JNJ) Presents at Barclays 28th Annual Global Healthcare Conference Transcript
Johnson & Johnson Announces U.S. FDA Approval of TECVAYLI® plus DARZALEX FASPRO® for Relapsed/Refractory Multiple Myeloma, Offering a Potential New Standard of Care as Early as Second Line
Approval based on unprecedented Phase 3 data demonstrating statistically significant improvements in progression – free survival and overall survival versus standard of care regimens 83.3% of patients...
US FDA approves JNJ's blood cancer drug
The U.S. Food and Drug Administration on Thursday approved Johnson & Johnson's treatment for a type of blood cancer, making it the third drug cleared under the agency's new speedy review prog...
Johnson & Johnson launches website for direct-to-consumer sales
Johnson & Johnson has launched a website to sell some of its drugs directly to U.S. patients who either don't have insurance or pay for their drugs out of pocket.
Johnson & Johnson (JNJ) Presents at TD Cowen 46th Annual Health Care Conference Transcript
Johnson & Johnson (JNJ) Presents at TD Cowen 46th Annual Health Care Conference Transcript
Wasatch Global Value Fund Q4 2025 Performance Review
Production volumes for Samsung's foundry business have been boosted by demand for HBM chips. Johnson & Johnson announced plans to spin its orthopedics business (joint replacements, surgical tools, etc...
Johnson & Johnson therapy nipocalimab granted U.S. FDA Fast Track designation in systemic lupus erythematosus (SLE)
Fast Track designation reflects the unmet need in this serious disease and enables the potential for an accelerated FDA review timeline The designation is supported by a Phase 2 study in which nipocal...
Johnson & Johnson to Host Investor Conference Call on First-Quarter Results
NEW BRUNSWICK, N.J.--(BUSINESS WIRE)--Johnson & Johnson (NYSE: JNJ) will host a conference call for investors at 8:30 a.m. (Eastern Time) on Tuesday, April 14th to review first-quarter results. Joaqui...
2 Dividend Kings That Could Easily Keep The Growth Streak Alive
We are looking at a screening process to sort out and look for some potential opportunities in the elite group known as the dividend kings. Dividend growers can help investors combat the erosion of bu...