152.75 -0.32 (-0.21%)
After hours: 6:30PM EST
Previous Close | 156.22 |
Open | 155.99 |
Bid | 152.36 x 800 |
Ask | 153.04 x 800 |
Day's Range | 151.47 - 156.10 |
52 Week Range | 109.16 - 173.65 |
Volume | 10,700,710 |
Avg. Volume | 8,213,858 |
Market Cap | 402.372B |
Beta (5Y Monthly) | 0.71 |
PE Ratio (TTM) | 27.78 |
EPS (TTM) | N/A |
Earnings Date | N/A |
Forward Dividend & Yield | 4.04 (2.59%) |
Ex-Dividend Date | Feb 22, 2021 |
1y Target Est | N/A |
Johnson & Johnson (NYSE: JNJ) (the Company) today announced that the U.S. Centers for Disease Control and Prevention's (CDC) Advisory Committee on Immunization Practices (ACIP) has recommended the first single-shot COVID-19 vaccine, developed by the Janssen Pharmaceutical Companies of Johnson & Johnson, for individuals 18 years of age and older under the Emergency Use Authorization (EUA) issued by the U.S. Food and Drug Administration (FDA).
Johnson & Johnson (NYSE: JNJ) (the Company) today announced that the U.S. Food and Drug Administration (FDA) has issued Emergency Use Authorization (EUA) for its single-dose COVID-19 vaccine, developed by the Janssen Pharmaceutical Companies of Johnson & Johnson, to prevent COVID-19 in individuals 18 years of age and older.
Johnson & Johnson (NYSE: JNJ) (the Company) today announced that the U.S. Food and Drug Administration's (FDA) Vaccines and Related Biological Products Advisory Committee (VRBPAC) unanimously voted to recommend Emergency Use Authorization (EUA) for the Company's single-shot COVID-19 vaccine candidate for adults 18 and older, developed by the Janssen Pharmaceutical Companies of Johnson & Johnson. The vote was based on a totality of scientific evidence provided by the Company, including efficacy and safety data from the Phase 3 ENSEMBLE trial.