Glenmark gets USFDA tentative nod for oral contraceptives
According to IMS Health sales data for the 12 months to February 2016, Lo Loestrin Fe achieved annual sales of around $432.2 million, Glenmark said.
Glenmark Pharmaceuticals USA has been granted tentative approval by the USFDA for Norethindrone Acetate and Ethinyl Estradiol tablets USP, 1 mg/0.01 mg, Ethinyl Estradiol tablets USP, 0.01 mg and Ferrous Fumarate tablets, 75 mg, the generic version of Lo Loestrin Fe, the company said in a BSE filing today.
It further said: "Glenmark will market this product upon receiving the final approval...The patent listed in the Orange Book for Lo Loestrin Fe tablets is scheduled to expire on February 22, 2029."
According to IMS Health sales data for the 12 months to February 2016, Lo Loestrin Fe achieved annual sales of around $432.2 million, Glenmark said.
The company's current portfolio consists of 112 products authorised for distribution in the US marketplace and 57 Abbreviated New Drug Applications (ANDA) pending for approval with the USFDA.
Shares of the company were trading 0.58 per cent up at Rs 835.25 on BSE.
COMMENTS
All Comments
By commenting, you agree to the Prohibited Content Policy
PostBy commenting, you agree to the Prohibited Content Policy
PostFind this Comment Offensive?
Choose your reason below and click on the submit button. This will alert our moderators to take actions