AbbVie Inc.

AbbVie Inc.

ABBV

$265.30

Updated: 24/09/2026, 05:35:28

Market Cap
$468.73B
Sector
Healthcare
Industry
Drug Manufacturers - General
Country
US
Stock valuation chart
One-year closing share-price history for ABBV
Company Profile

AbbVie Inc. is a global biopharmaceutical company dedicated to the discovery, development, manufacturing, and commercialization of advanced medicines. Its extensive therapeutic portfolio encompasses several key areas: Immunology and Inflammation: Leading products include HUMIRA, an injectable therapy for autoimmune and intestinal Behçet's diseases; SKYRIZI, which addresses moderate to severe plaque psoriasis in adults; and RINVOQ, a JAK inhibitor for moderate to severe active rheumatoid arthritis in adult patients. Oncology and Hematology: For blood cancers, AbbVie provides IMBRUVICA and VENCLEXTA (a BCL-2 inhibitor), both indicated for adult patients with chronic lymphocytic leukemia (CLL) and small lymphocytic lymphoma (SLL). Virology: MAVYRET offers a treatment option for individuals with chronic HCV genotype 1-6 infection. Gastroenterology and Endocrinology: The company supplies CREON, an enzyme replacement therapy for exocrine pancreatic insufficiency, and Synthroid, used to manage hypothyroidism. Linzess/Constella helps treat irritable bowel syndrome with constipation (IBS-C) and chronic idiopathic constipation. Women's Health and Urology: Lupron serves as a palliative treatment for conditions like advanced prostate cancer, endometriosis, central precocious puberty, and anemia caused by uterine fibroids. ORILISSA, a nonpeptide small molecule GnRH antagonist, is designed for women experiencing moderate to severe endometriosis pain. Neurology: AbbVie offers Duopa and Duodopa, a levodopa-carbidopa intestinal gel for Parkinson's disease, and Ubrelvy to treat migraines (with or without aura) in adults. The therapeutic formulation of Botox is also part of its offerings. Ophthalmology: Its eye care segment features Lumigan/Ganfort (a bimatoprost ophthalmic solution) and Alphagan/Combigan (an alpha-adrenergic receptor agonist), both aimed at reducing elevated intraocular pressure (IOP) in patients with open-angle glaucoma (OAG) or ocular hypertension. Restasis, a calcineurin inhibitor immunosuppressant, is provided to enhance tear production, alongside other specialized eye care products. AbbVie Inc. also engages in research collaborations, including a partnership with Dragonfly Therapeutics, Inc. The company was founded in 2012 and operates from its headquarters in North Chicago, Illinois.

USD
NYSE
CEO: Robert A. Michael
Employees: 57,000
https://www.abbvie.com
Asset Summaries
Latest generated summaries for ABBV

No summaries found.

Detailed business
Evidence-backed facts extracted from the latest official annual filing.
ABBV-10-k-fy2025.html3.6 MBtext/htmlENFiled 20/02/2026Period ended 31/12/2025

Business monitoring

Reported and calculated KPIs plus operational exposure disclosed in the FY 2025 filing.

Evidence-backed · 52 KPI observations

Revenue

$61.2B

FY 2025 · Reported

Net income

$4.2B

FY 2025 · Reported

Gross margin

70.2%

FY 2025 · Calculated

Free cash flow

$17.8B

FY 2025 · Calculated

R&D intensity

N/A

FY — · Reported

Share repurchases

$1.0B

FY 2025 · Reported

Earnings and cash generation
USD billions, directly sourced from inline XBRL; free cash flow is operating cash flow less capex.
Profitability and reinvestment
Margins and R&D as a percentage of revenue.
Top products and services
Products and services mentioned in the filing; a quantitative sales breakdown was not disclosed.

Other offerings mentioned without separate sales

Key on-market growth products

Area-level product sales are displayed only when the filing reports a product × geography breakdown. Regional totals are not allocated across products by estimation.

Geographic footprint
What the filing identifies, separated by location role so partner manufacturing is not presented as Apple-owned factories.
1 named headquarters
0 manufacturing countries
0 individually named factories

Map layer

Pins show disclosed operations. The heatmap colors the filing’s reported geographies; regional figures shade the region and are not estimates for each country.

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Named headquarters Manufacturing partner country

Only locations and quantities explicitly supported by the filing are displayed. A country-level manufacturing percentage or product allocation is shown only when the source discloses it; materiality scores are never presented as production shares.

How the business makes money

Company overview

Global diversified research-based biopharmaceutical company; leadership in immunology, neuroscience, oncology, aesthetics

98%
Source evidence
“AbbVie is a global, diversified research-based biopharmaceutical company positioned for success with a comprehensive product portfolio that has leadership positions across immunology, neuroscience, oncology and aesthetics.”

Segment structure

AbbVie operates as a single global business segment

97%
Source evidence
“AbbVie operates as a single global business segment.”

Distribution channels

Products sold worldwide to wholesalers, distributors, government agencies, health care facilities, specialty pharmacies and independent retailers; certain products sold directly to physicians

95%
Source evidence
“AbbVie's products are generally sold worldwide directly to wholesalers, distributors, government agencies, health care facilities, specialty pharmacies and independent retailers from AbbVie-owned distribution centers and public warehouses.”

Key on-market growth products

Key on-market products: Skyrizi, Rinvoq, Vraylar, Botox Therapeutic, Ubrelvy, Qulipta, Vyalev, Venclexta, Elahere, Botox Cosmetic, Juvederm Collection

97%
Source evidence
“Maximizing revenue growth of our key on-market products, including Skyrizi, Rinvoq, Vraylar, Botox Therapeutic, Ubrelvy, Qulipta, Vyalev, Venclexta, Elahere, Botox Cosmetic and Juvederm Collection.”

Positioning and strategy

ImmunoGen acquisition

Acquired ImmunoGen (Feb 12, 2024) for $31.26/share, $9.8B total consideration ($9.2B net); ADC oncology platform incl. Elahere

96%
Source evidence
“On February 12, 2024, AbbVie completed its acquisition of ImmunoGen, Inc. (ImmunoGen). ImmunoGen is a commercial-stage biotechnology company focused on the discovery, development and commercialization of antibody-drug conjugates (ADC) for cancer patients.”

Cerevel Therapeutics acquisition and Pfizer license

Cerevel Therapeutics acquisition expanded neuroscience pipeline; assumed Pfizer license with up to $1.6B milestone payments; $4.5B emraclidine impairment

94%
Source evidence
“AbbVie could make additional payments of up to $1.6 billion upon achievement of certain regulatory and commercial milestones for all programs. Additionally, AbbVie will pay tiered royalties on net revenues.”

US capital investment projects

2025-2026 US investments: API facility in Illinois, biologics manufacturing/R&D expansion in Massachusetts, device manufacturing facility acquisition in Arizona

95%
Source evidence
“In 2025, AbbVie announced the start of construction of a new active pharmaceutical ingredient facility in Illinois and an expansion of biologics manufacturing and research and development capacity in Massachusetts. In January 2026, AbbVie announced that it entered into an agreement to acquire a device manufacturing facility in Arizona.”

R&D investment and pipeline

Continued investment in all stages of pipeline; late-stage milestones and key regulatory submissions/approvals expected in next 12 months

93%
Source evidence
“AbbVie anticipates several regulatory submissions, approvals and data readouts from key clinical trials in the next 12 months.”

2026 strategic objectives

2026 objectives: diversified revenue base, commercial execution, pipeline expansion incl. obesity, cash flow and dividend growth with investment grade rating

96%
Source evidence
“continuing to invest in and expand its pipeline in support of opportunities across our core areas of immunology, neuroscience, oncology and aesthetics as well as new sources of growth such as obesity”

Risks, financing, and outlook

2025 cost items

2025 costs: $7.4B intangible amortization, $6.5B contingent consideration fair value change, $847M intangible impairment, $276M acquisition/integration

96%
Source evidence
“(i) $7.4 billion related to the amortization of intangible assets; (ii) $6.5 billion for the change in fair value of contingent consideration liabilities; (iii) $847 million related to intangible asset impairment; and (iv) $276 million of acquisition and integration expenses.”

Contractual obligations as of December 31, 2025

Long-term debt $64,503M total; interest on long-term debt $35,243M; contingent consideration $25,374M (in millions)

95%
Source evidence
“Long-term debt, including current portion$64,503 $6,000 $58,503 Interest on long-term debt(a) 35,243 2,712 32,531 Contingent consideration liabilities(b) 25,374 3,455 21,919”

Short-term borrowings

Short-term borrowings: $2.0B 364-day term loan and $499M commercial paper as of December 31, 2025

95%
Source evidence
“Short-term borrowings included $2.0 billion of a 364-day term loan and $499 million of commercial paper, which are classified as current liabilities as of December 31, 2025.”

2025 financial results summary

2025: net revenues $61.2B (+9%), operating earnings $15.1B, diluted EPS $2.36, operating cash flows $19.0B

97%
Source evidence
“delivering worldwide net revenues of $61.2 billion, operating earnings of $15.1 billion, diluted earnings per share of $2.36 and cash flows from operations of $19.0 billion. Worldwide net revenues increased by 9% on a reported and on a constant currency basis.”

Quarterly dividend increase

Quarterly dividend increased ~5.5% from $1.64 to $1.73 per share beginning February 17, 2026

96%
Source evidence
“declared an increase in the company’s quarterly dividend from $1.64 per share to $1.73 per share beginning with the dividend payable on February 17, 2026 to stockholders of record as of January 16, 2026. This reflects an increase of approximately 5.5% over the previous quarterly rate.”

Tax items and unrecognized tax benefits

One-time transition tax liability $1.1B; unrecognized tax benefits $5.6B as of December 31, 2025

93%
Source evidence
“Liabilities for unrecognized tax benefits totaled $5.6 billion as of December 31, 2025.”

Rinvoq generic settlement

Rinvoq tablet generic settlement: no US generic entry expected prior to April 2037 (assuming pediatric exclusivity)

96%
Source evidence
“no generic entry for any Rinvoq tablets is expected prior to April 2037 in the United States.”

One Big Beautiful Bill Act of 2025

2025 Act restored domestic R&D expensing and had a favorable impact on cash tax payments in the current year

92%
Source evidence
“The new legislation had a favorable impact on cash tax payments in the current year.”

IRA Medicare price-setting selections

IRA government-set prices: Imbruvica (2026), Vraylar and Linzess (2027), Botox (2028)

95%
Source evidence
“In 2023, the U.S. Department of Health and Human Services, through Centers for Medicare and Medicaid Service, selected Imbruvica as one of 10 medicines subject to government-set prices in Medicare Part D beginning in 2026 and in 2025, selected Vraylar and Linzess as two of 15 medicines subject to government-set prices in Medicare Part D beginning in 2027. In January 2026, Botox was selected as one of 15 medicines subject to government-set prices in Medicare Parts B and D beginning in 2028.”

US government pricing agreement (post-2025)

Voluntary agreement with U.S. government: Medicaid low prices, $100B US R&D/capital investment pledge over next decade, three-year tariff/price-mandate exemption

95%
Source evidence
“AbbVie pledged $100 billion in U.S.-based research and development and capital investments, including manufacturing, over the next decade. Under this voluntary agreement, the U.S. government has agreed to provide AbbVie a three-year exemption from tariffs and future price mandates.”

Global regulatory approval requirements

Multi-jurisdiction regulatory requirements: FDA, EU EMA centralized procedure, Japan PMDA, China NMPA with local clinical data; local studies required in South Korea, Taiwan, India, Russia

93%
Source evidence
“certain countries (notably South Korea, Taiwan, India and Russia) also generally require that clinical studies that include data from patients in those countries be conducted in order to support local regulatory approval.”

Patent expiration and biosimilar competition risk

Patent expiration/generic and biosimilar competition may significantly reduce product sales in a short amount of time

97%
Source evidence
“The expiration or loss of patent protection for a product typically is followed promptly by substitutes that may significantly reduce sales for that product in a short amount of time.”

Debt obligations risk

Debt obligations could require cash flow for interest, reduce funds for capex and growth, and refinancing risk exists

94%
Source evidence
“requiring a portion of AbbVie's cash flow from operations to make interest payments on this debt and reducing the cash flow available to fund capital expenditures and other corporate purposes and to grow AbbVie's business.”

IT, cybersecurity and AI risk

Cybersecurity threats to healthcare data; failure to adopt emerging technologies such as AI could hinder competitiveness

94%
Source evidence
“AbbVie utilizes AI and other emerging technologies in select applications to support its operations. These technologies may present opportunities for AbbVie's business but may also entail risks, including that AI-generated analyses utilized by AbbVie could be deficient or exacerbate regulatory, cybersecurity or other significant risks.”

Pricing pressure and cost containment

Government and private-sector cost containment and pricing pressure expected to continue in US and internationally

93%
Source evidence
“Political and budgetary pressures in the United States and in other countries may also heighten the scope and severity of pricing pressures on AbbVie's products for the foreseeable future.”

Material exposure graph

Rinvoq
Revenue Exposure

Rinvoq is a key growth product; with Skyrizi it represented approximately 42% of 2025 net revenues; generic entry settled to no earlier than April 2037 in the US.

Relevance 95·Dependency 85·Confidence 97
Source evidence
“Skyrizi and Rinvoq each represented greater than 10% of AbbVie's total net revenues and, in aggregate, these products accounted for approximately 42% of total net revenues in 2025.”
Skyrizi
Revenue Exposure

Skyrizi is a top growth product; together with Rinvoq it represented approximately 42% of 2025 total net revenues.

Relevance 95·Dependency 85·Confidence 97
Source evidence
“Skyrizi and Rinvoq each represented greater than 10% of AbbVie's total net revenues and, in aggregate, these products accounted for approximately 42% of total net revenues in 2025.”
Wholesale distributors (McKesson, Cardinal Health, Cencora)
Customer Exposure

Substantially all US pharmaceutical product sales flow through three wholesale distributors; their financial difficulty would adversely affect AbbVie's business.

Relevance 90·Dependency 90·Confidence 97
Source evidence
“In 2025, three wholesale distributors (McKesson Corporation, Cardinal Health, Inc. and Cencora, Inc.) accounted for substantially all of AbbVie's pharmaceutical product sales in the United States.”
United States
Geopolitical Exposure

US government pricing agreement, IRA price-setting, tariff exemption, and $100B US R&D/capital investment pledge tie AbbVie closely to US policy and market.

Relevance 90·Dependency 80·Confidence 93
Source evidence
“Subsequent to December 31, 2025, AbbVie announced a voluntary agreement with the U.S. government to further advance access and affordability of AbbVie’s products in the U.S. while protecting and investing in U.S. pharmaceutical innovation.”
Inflation Reduction Act of 2022
Regulatory Exposure

IRA creates inflation penalties, Medicare Part D redesign shifting costs to manufacturers, and government price-setting for certain Part B and Part D drugs affecting multiple AbbVie products.

Relevance 85·Dependency 65·Confidence 95
Source evidence
“The Inflation Reduction Act of 2022 has and will continue to have a significant impact on how drugs are covered and paid for under the Medicare program, including through the creation of financial penalties for drugs whose price increases outpace inflation, the redesign of Medicare Part D benefits to shift a greater portion of the costs to manufacturers, and through government price-setting for certain Medicare Part B and Part D drugs.”
Botox
Regulatory Exposure

Botox was selected in January 2026 for government-set prices under Medicare Parts B and D beginning in 2028 under the IRA.

Relevance 70·Dependency 55·Confidence 94
Source evidence
“In January 2026, Botox was selected as one of 15 medicines subject to government-set prices in Medicare Parts B and D beginning in 2028.”
Active pharmaceutical ingredients
Supplier Dependency

Commercialization depends on API and finished product being manufactured in sufficient quantities compliant with FDA and foreign regulatory requirements; AbbVie is investing in a new US API facility.

Relevance 65·Dependency 60·Confidence 85
Source evidence
“ensuring that the active pharmaceutical ingredient(s) for a product and the finished product are manufactured in sufficient quantities and in compliance with requirements of the FDA and similar foreign regulatory agencies and with acceptable quality and pricing to meet commercial demand”
Imbruvica
Regulatory Exposure

Imbruvica selected as one of 10 medicines subject to government-set Medicare Part D prices beginning in 2026.

Relevance 65·Dependency 55·Confidence 94
Source evidence
“selected Imbruvica as one of 10 medicines subject to government-set prices in Medicare Part D beginning in 2026”
Elahere
Demand Driver

Elahere, a first-in-class ADC acquired via ImmunoGen, is a key on-market growth product for platinum-resistant ovarian cancer.

Relevance 60·Dependency 45·Confidence 92
Source evidence
“Maximizing revenue growth of our key on-market products, including Skyrizi, Rinvoq, Vraylar, Botox Therapeutic, Ubrelvy, Qulipta, Vyalev, Venclexta, Elahere, Botox Cosmetic and Juvederm Collection.”
Antibody-drug conjugates (ADC)
Technology Dependency

The ImmunoGen acquisition brought AbbVie an ADC technology platform and enhanced its ADC development efforts in oncology.

Relevance 55·Dependency 45·Confidence 90
Source evidence
“ImmunoGen is a commercial-stage biotechnology company focused on the discovery, development and commercialization of antibody-drug conjugates (ADC) for cancer patients.”
Artificial intelligence
Competitive Exposure

AbbVie's failure to effectively implement AI and emerging technologies could hinder competitiveness as competitors' AI advancements lead to more efficient operations.

Relevance 45·Dependency 35·Confidence 90
Source evidence
“our failure to effectively implement these technologies could hinder our ability to compete, as competitors' advancements in AI may lead to more efficient operations.”
Full company information
Latest profile, trading, valuation, and identifier data stored for ABBV.
Share price
$265.30
Market cap
$468.73B
Exchange
NYSE
Currency
USD
CEO
Robert A. Michael
Employees
57,000
IPO date
02/01/2013
Beta
0.281
Last dividend
$0.00
Day range
$263.59 – $269.39
52-week range
$190.75 – $269.39
1-day performance
0.03%
1-year performance
39.08%
Current drawdown (1Y)
-1.52%
CIK
0001551152
CUSIP
00287Y109
ISIN
US00287Y1091
Created
07/12/2025, 01:53:09
Last update
24/09/2026, 05:35:28

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