Trimeprazine with Prednisolone Tablets, the generic equivalent of Temaril-P (Zoetis), will be displayed at this year’s ...

Lupin has received USFDA approval to market a generic HIV medication in the US market, under the PEPFAR program. The drug ...

The US Food and Drug Administration (FDA) has approved the abbreviated new drug application (ANDA) of Lupin’s Sacubitril and ...

Drug firm Lupin on Friday said it has received approval from the US health regulator to market a generic HIV medication in ...

particularly when a patient receives a drug from multiple manufacturers. The FDA sets strict standards for the approval of generic equivalents, as do other western countries. Generics must contain ...

The three largest pharmacy benefit managers (PBMs) inflated the price of specialty generic drugs beyond their costs of ...

The single-dose ampules is bioequivalent and therapeutically equivalent to the reference listed drug, Vitamin K1 Injectable ...

An Abbreviated New Drug Application (ANDA) is an application submitted to the U.S. FDA to demonstrate that a generic drug is equivalent to a previously approved Reference Listed Drug (RLD) in terms of ...

Some of China’s senior doctors are raising concern over the quality of domestic generic medicines that have largely replaced western brand-name drugs at hospitals, amid a rare public backlash ...

Cigna (CI) and UnitedHealth (UNH) significantly marked up prices for specialty generic drugs over a six-year period.

Hopefully, the approval will help prevent shortages triggered by demand for injectable weight loss drugs such as semaglutide (Ozempic, Wegovy) and tirzepatide (Mounjaro, Zepbound) There is still no ...