The proposal was originally submitted by the National Federation of Farmers’ Procurement, Processing and Retailing Cooperatives of India Ltd (NACOF), which had sought permission to open 58 outlets in ...

This latest FDA program aims to provide speedier reviews for generic drugmakers who produce their products in the U.S.

The U.S. Food and Drug Administration said on Friday that it has launched a new pilot program to speed up the review process for generic drugs that are tested and manufactured entirely in the United ...

Reshoring generic pharmaceutical production is essential in today’s era of geopolitical instability and heightened awareness ...

The FDA is in the process of approving the inexpensive, generic drug derived from folic acid to help children diagnosed with ...

This week, the Trump administration announced that the FDA had approved leucovorin, a generic drug, as a treatment for autism ...

This week, the FDA began the process of approving leucovorin, an inexpensive, generic drug derived from folic acid, to help children diagnosed with autism.

The theory behind leucovorin's use for autism postulates that some children have a blockage in the transport of folic acid into the brain that potentially contributes to neurological symptoms.

A generic version of Wegovy is not currently available in the United States due to existing patents held by the manufacturer, Novo Nordisk, that may be active until 2041. When the U.S. patent for ...

In taking the unusual step of approving an old generic drug as a treatment for autism, the Food and Drug Administration stunned some experts by departing sharply from the agency’s typical standard for ...

Andrew Joseph covers health, medicine, and the biopharma industry in Europe. You can reach Andrew on Signal at drewqjoseph.45. Daniel Payne reports on how the health industry and Washington influence ...