J&J Seeks FDA Approval for Tremfya for Psoriasis in Kids
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Express News | J&J: Mentor Memorygel Enhance Breast Implant Receives FDA Approval for Largest Size Breast Implants for Reconstruction
Express News | Johnson & Johnson Seeks U.S. FDA Approval for First Pediatric Indications for Tremfya® (Guselkumab)
Express News | France has issued guidelines to support businesses in using ai.
Express News | The annual pharmaceutical imports value of Peking Tianzhu Comprehensive Bonded Zone is approximately 120 billion yuan.
Express News | Two innovative drugs from johnson & johnson have been included in the new national medical insurance catalog.
Investors in Johnson & Johnson (NYSE:JNJ) Have Seen Decent Returns of 30% Over the Past Five Years
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J&J Seeks FDA Nod for Subcutaneous Tremfya as Induction Regimen in UC
Johnson & Johnson To Go Ex-Dividend On November 26th, 2024 With 1.24 USD Dividend Per Share
November 24th (Eastern Time) - $Johnson & Johnson(JNJ.US)$ is trading ex-dividend on November 26th, 2024.Shareholders of record on November 26th, 2024 will receive 1.24 USD dividend per share on
Johnson & Johnson (JNJ.US) has submitted a regulatory application to the FDA for its antibody therapy to treat moderate to severe active ulcerative colitis.
Johnson & Johnson (JNJ.US) announced that it has submitted a supplemental Biological Product License Application (sBLA) to the FDA in the USA.
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Express News | Johnson & Johnson is seeking approval from the FDA to use the subcutaneous induction therapy of TREMFYA (GUSELKUMAB) to treat ulcerative colitis.
Johnson & Johnson Applies for FDA Approval of Tremfya Subcutaneous Induction Regimen for Ulcerative Colitis