BMY

BMY

USD

Bristol-Myers Squibb Company Common Stock

$47.170+0.400 (0.855%)

Reaalajas hind

Healthcare
Drug Manufacturers - General
Ameerika Ühendriigid

Hinnagraafik

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Põhinäitajad

Turunäitajad
Ettevõtte fundamentaalnäitajad
Kauplemisstatistika

Turunäitajad

Avatud

$46.770

Kõrge

$47.420

Madal

$46.650

Maht

12.61M

Ettevõtte fundamentaalnäitajad

Turukapitalisatsioon

96.0B

Tööstusharu

Drug Manufacturers - General

Riik

United States

Kauplemisstatistika

Keskmine maht

14.87M

Börs

NYQ

Valuuta

USD

52 nädala vahemik

Madal $41.61Praegune $47.170Kõrge $63.33

Seotud uudised

Reuters

Bristol Myers, Pfizer to sell blood thinner Eliquis directly to patients

US drugmakers Bristol Myers and Pfizer said on Thursday that they will make their blood thinner, Eliquis, available directly to cash-paying patients at discounted rate through a new program.

Vaata rohkem
Bristol Myers, Pfizer to sell blood thinner Eliquis directly to patients
BusinessWire

Bristol Myers Squibb and Pfizer Announce Direct-to-Patient Eliquis® (apixaban) Option

Eliquis 360 Support Program Now Offers Eliquis to Cash-Paying Patients at More than 40% Discount to Current List Price The Bristol Myers Squibb-Pfizer (NYSE:BMY) – (NYSE:PFE) Alliance today announced a new

Vaata rohkem
Bristol Myers Squibb and Pfizer Announce Direct-to-Patient Eliquis® (apixaban) Option
CNBC

Healthy Returns: Medicaid cuts in Trump’s megabill may affect some drugmakers more than others

Trump's "big beautiful" bill will also affect the pharmaceutical industry, while AI startups have pulled in the majority of digital health funding this year.

Vaata rohkem
Healthy Returns: Medicaid cuts in Trump’s megabill may affect some drugmakers more than others
BusinessWire

U.S. Food and Drug Administration Approves Streamlined Patient Monitoring Requirements and Removal of REMS Programs within Bristol Myers Squibb's Cell Therapy Labels

Label updates reflect growing body of real-world evidence and regulatory confidence in the safety profile of the class of CD19- and BCMA-directed autologous CAR T cell therapies, reinforcing efforts to increase

Vaata rohkem
U.S. Food and Drug Administration Approves Streamlined Patient Monitoring Requirements and Removal of REMS Programs within Bristol Myers Squibb's Cell Therapy Labels

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