[ad_1] Alembic Pharmaceuticals Limited has announced that it has received final USFDA approval for its Abbreviated New Drug Application (ANDA) for Nifedipine Extended-Release Tablets USP, 30 mg, 60 mg and 90 mg. USFDA approved ANDA therapeutically approved by Pfizer Inc. equivalent to the company’s Procardia XL Extended-Release tablets, 30 mg, 60 mg and 90 mg. … Read more
[ad_1] November 17: Shri Kiranbhai Lalluvhai Patel, Joint Managing Director, ASPEE Group, has been conferred with the prestigious Lifetime Achievement Citation at the Education Leadership Award for the year 2022-23 by Shiksha Vishwa. Honorable awards came to him in recognition of his immense contribution to the development of schools and colleges in India. The award … Read more
[ad_1] November 17: Shri Kiranbhai Lalluvhai Patel, Joint Managing Director, ASPEE Group, has been conferred with the prestigious Lifetime Achievement Citation in Education Leadership Award for the year 2022-23 by Shiksha Vishwa. Honorable awards came to him in recognition of his immense contribution to the development of schools and colleges in India. The award ceremony … Read more
[ad_1] MT Newswires 2022 All news about ABBVIE INC. Analyst Recommendations on ABBVIE INC. Sale 2022 58 298 M – – Net income 2022 13 952 M – – Net debt 2022 54 043 M – – P/E ratio 2022 18.4x Harvest 2022 3.73% Capitalization 271 B 271 B … Read more
[ad_1] Ascletis Pharma’s monkeypox treatment has received approval from the US Food and Drug Administration (FDA) for a New Drug (IND) application. The FDA made its decision based on the available data, and Askletis can now proceed to a Phase 1b clinical trial to evaluate the safety, tolerability, efficacy and pharmacokinetics of the pill in … Read more
[ad_1] Zydus Lifesciences has received approval from the United States Food and Drug Administration (USFDA) for Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP, 2.5 mg/6.25 mg, 5 mg/6.25 mg, 10 mg/6.25 mg (USRLD : Ziac tablets) received final marketing approval. The combination of bisoprolol fumarate and hydrochlorothiazide is indicated for the treatment of high blood pressure … Read more
[ad_1] Business standard Lupine today announced that it has received tentative approval from the United States Food and Drug Administration (FDA) for its Abbreviated New Drug Application (ANDA), Drospirenone Tablets, 4 mg, to market the generic equivalent of Exeltis, Slind Tablets, 4 … Read more
[ad_1] Glenmark Pharmaceuticals Limited has received final approval from the United States Food and Drug Administration (US FDA) for Sodium Phenylbutyrate Tablets USP, 500 mg, Generic Version Buphenyl Tablets, 500 mg, Horizon Therapeutics, LLC. According to the filings, Glenmark’s Sodium Phenylbutyrate Tablets USP, 500 mg, is distributed in the USA by Glenmark Pharmaceuticals Inc., USA. … Read more
[ad_1] The Ontario government is investing $2.5 million to accelerate the expansion plans of the Royal Victoria Regional Health Center (RVH) for its southern campus in Innisfil. “We are going to add more operating rooms, more beds and a new hospital in Innisfil,” said RVH President and CEO Janice Skot. Premier Doug Ford stopped by … Read more
[ad_1] January 28, 2022 The Minister for Health and HIV / Aids Jelta Wong shared in the knowledge and concerns raised by the Wanzing family, and the anxiety that comes from the time required for the investigation to be properly carried out in the death of the his son In a statement released late yesterday, … Read more