The FDA has granted marketing authorization to CT-132, an adjunctive, prescription digital therapeutic for the preventive ...

From Crohn disease to uncomplicated urinary tract infections and beyond, the FDA issued several high-impact drug approvals last month.

V Men’s multivitamin is being recalled due to undeclared soy, a potential allergen, according to the FDA. Here’s a list of ...

Click Therapeutics has collected a groundbreaking green light from the FDA for the agency’s first prescription digital ...

According to the FDA, while allergic reactions to color additives are rare, dyes must be included in product labels.

Target recalled 26,500 units of Good & Gather baby Pea, Zucchini, Kale & Thyme Vegetable Purèe for elevated lead levels.

In an hour-long meeting at Eli Lilly and Company’s headquarters in Indianapolis on April 15, the pharmaceutical company’s top ...

The FDA has labeled this recall as a Class II risk. The administration explains that this designation is “a situation in ...

SSRI medications have come under scrutiny as of late, despite medical experts maintaining they're safe and effective.

Miami-based food manufacturer Fruselva issued a voluntary recall of 25,600 units of four-ounce packages of Good & Gather baby Pea Zucchini Kale & Thyme Vegetable Puree on March 12. The lot numbers and ...

U.S. Food and Drug Administration Commissioner Martin Makary announced on Thursday a policy to limit employees of companies ...

A three-judge panel wrestled Thursday with Novartis AG’s challenge against the FDA over its approval of a generic version of ...