The move comes more than 30 years since the Food and Drug Administration prohibited the use of Red No. 3 in cosmetics after ...
The Food and Drug Administration has given Lupin a tentative nod for two new generics. The first medication is loteprednol etabonate ophthalmic gel, 0.38%, which is a generic of Bausch & Lomb’s ...
Ivacaftor Oral Granules, 25 mg, 50 mg and 75 mg per unit dose packet are indicated for cystic fibrosis treatment in patients aged 4 months and older. Mumbai: Global pharma major, Lupin Limited, has ...
Global pharma major Lupin Limited (Lupin) announced that it has received tentative approval from the United States Food and Drug Administration (FDA) for its Abbreviated New Drug Application for ...
This move came after Lupin announced that it got tentative approval from the US Food and Drug Administration for its drug for cystic fibrosis treatment known as Ivacaftor oral granules. The product ...
Lupin Ltd. announced that it has received tentative approval from the US Food and Drug Administration to launch its generic version of Ivacaftor oral granules, used in the treatment of cystic fibrosis ...
Global pharmaceutical giant Lupin has announced that it has received tentative approval from the United States Food and Drug Administration (US FDA) for its Abbreviated New Drug Application (ANDA) for ...
The approval granted by the US Food and Drug Administration (USFDA) is for the abbreviated new drug application for Ivacaftor oral granules of strengths 25 mg, 50 mg, and 75 mg per unit dose packet, ...
Lupin Ltd announced on Thursday a tentative nod from the USFDA to market its generic version of Ivacaftor oral granules, designed for cystic fibrosis treatment. The US approval pertains to various ...
New Delhi, Jan 9 (PTI) Pharma major Lupin Ltd on Thursday said it has received tentative approval from the US health regulator to market its generic version of Ivacaftor oral granules used in ...
Hyderabad, Jan 9 (UNI) Global pharma major Lupin Limited (Lupin) on Thursday announced that it has received tentative approval from the United States Food and Drug Administration (U.S. FDA) for its ...