TEVA

Teva Pharma Industries Ltd ADR
NYSEHEALTHCAREDRUG MANUFACTURERS - SPECIALTY & GENERIC

Key Statistics

Market Cap
$42.37B
P/E Ratio
60.60
EPS
$0.60
Beta
0.87
52W High
$38.37
52W Low
$18.21
50-Day MA
$34.61
200-Day MA
$32.57
Dividend Yield
Profit Margin
4.08%
Forward P/E
11.88
PEG Ratio
0.67

About Teva Pharma Industries Ltd ADR

Teva Pharmaceutical Industries Limited, a pharmaceutical company, develops, manufactures, markets, and distributes generic drugs, specialty drugs, and biopharmaceuticals in North America, Europe, and internationally. The company is headquartered in Petach Tikva, Israel.

Official WebsiteUSAFY End: December

Fundamentals

Revenue (TTM)$17.32B
Gross Profit (TTM)$9.08B
EBITDA$4.27B
Operating Margin4.03%
Return on Equity9.69%
Return on Assets5.13%
Revenue/Share (TTM)$15.00
Book Value$6.65
Price-to-Book5.50
Price-to-Sales (TTM)2.45
EV/Revenue3.241
EV/EBITDA17.80
Quarterly Earnings Growth (YoY)72.20%
Quarterly Revenue Growth (YoY)-0.80%
Shares Outstanding$1.17B
Float$1.09B
% Insiders0.00%
% Institutions64.48%

Historical Volatility

HV 10-Day
33.90%
HV 20-Day
28.24%
HV 30-Day
36.19%
HV 60-Day
36.65%
HV Rank
46.4%

Volatility is currently contracting

Analyst Ratings

Consensus ($41.60 target)
4
Strong Buy
7
Buy
1
Hold

Latest News

Teva Announces Launch of Offering of Senior Notes

TEL AVIV, Israel, Sept. 07, 2026 (GLOBE NEWSWIRE) -- Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) (“Teva”) announced today its intention to issue senior notes through its special purpose finance subsidiaries. Teva Pharmaceutical Finance Netherlands II B.V. (“Teva Finance II”) intends to offer EUR-denominated Senior Notes (the “Euro Notes”) and Teva Pharmaceutical Finance Netherlands III B.V. (“Teva Finance III”) and Teva Pharmaceutical Finance Netherlands IV B.V. (“Teva Finance IV” and, together with Teva Finance II and Teva Finance III, the “Issuers”) intend to offer USD-denominated Senior Notes (the “USD Notes” and, together with the Euro Notes, the “Notes”).

GlobeNewsWire9/7/2026Neutral
Teva and Trump Administration Announce Intent to Reach Agreement around Affordable Medicines and Supply Chain Security for Patients in the U.S.

PARSIPPANY, N.J. and TEL AVIV, Israel, Aug. 31, 2026 (GLOBE NEWSWIRE) -- Teva Pharmaceuticals, a U.S. affiliate of Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA), today announced a shared commitment with the Trump Administration to lower the cost of select medicines for American patients covered by Medicaid. When finalized, this agreement will support continued investment in scientific innovation and pharmaceutical manufacturing capabilities.    “Teva appreciates the opportunity to work with President Trump and his Administration to expand access and affordability for patients today while enabling continued investment in medicines patients need tomorrow,” said Chris Fox, President, Teva USA. “Teva built its business around delivering affordable medicines to Americans, and we share the Administration's commitment to improve access to more affordable medicines while investing in scientific innovation and domestic manufacturing capabilities in the U.S.”                                                                                                  Teva remains in active discussions with the Trump Administration to strike a deal anchored in all four of the President's drug pricing priorities. If an agreement is reached, Teva would align U.S. Medicaid pricing for select medicines with pricing in leading developed markets through the GENEROUS (GENErating cost Reductions fOr U.S. Medicaid) framework. The agreement also would include a prospective Most-Favored-Nation (MFN) commitment for applicable future innovative product launches.  Additionally, Teva has offered a dedicated reserve of certain active pharmaceutical ingredients (API) in support of public health needs and continued investment into U.S. pharmaceutical manufacturing capabilities. Conditions of the negotiation to reach a final agreement remain confidential.

GlobeNewsWire8/31/2026Neutral
Teva Announces Proposed Acquisition of a Novel Neuroscience Product Reinforcing Disciplined Business Development Approach Under Pivot to Growth Strategy

BXCL501, a novel dexmedetomidine sublingual film, is under FDA review for potential at-home (outpatient) use for the acute treatment of agitation associated with schizophrenia or bipolar I or II disorder in adults.  Agreement is part of a court-supervised sale process with BioXcel Therapeutics, Inc. and remains subject to bankruptcy court approval, potential higher bids, and customary closing conditions.

GlobeNewsWire8/28/2026Neutral

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Data last updated: 9/7/2026