Business Standard

Ranbaxy gets USFDA nod for Loperamide

Image

Our Web Bureau Mumbai
Ranbaxy gets USFDA nod for Loperamide
Our Web Bureau / Mumbai September 11, 2006
Ranbaxy Laboratories has received approval from the US Food and Drug Administration (USFDA) to manufacture and market Loperamide Hydrochloride and Simethicone Tablets, 2 mg/125 mg.

According to a release issued by Ranbaxy to the BSE today, the Office of Generic Drugs, USFDA, has determined the company's Loperamide Hydrochloride and Simethicone Tablets to be bioequivalent to the reference listed drug (RLD) Imodium

Don't miss the most important news and views of the day. Get them on our Telegram channel

First Published: Sep 11 2006 | 12:28 PM IST

Explore News