Zydus Cadila gets USFDA approval for Esomeprazole Magnesium delayed-release capsules
The company said Esomeprazole belongs to the group of medicines termed as proton pump inhibitors.
New Delhi: Zydus Cadila has received final approval from the US health regulator to market Esomeprazole Magnesium delayed-release capsules, used to treat acid reflux. The approval has been granted in the strengths of 25 mg and 40 mg, the company said in a BSE filing.
Zydus Cadila said the drug will be produced at the group's formulations manufacturing facility at Ahmedabad.
The company said Esomeprazole belongs to the group of medicines termed as proton pump inhibitors.
Also Read: Zydus Cadila gets USFDA nod for Chlorthalidone tablets to treat high BP
Esomeprazole reduces the amount of acid secreted by the stomach.
The group has more than 266 approvals and so far filed over 350 abbreviated new drug applications (ANDAs) since it started filings in 2003-04.
Also Read: CDSCO approves Zydus, SIFI pact to launch Intraocular Lenses in India
Farhat Nasim joined Medical Dialogue an Editor for the Business Section in 2017. She Covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She is a graduate of St.Xavier’s College Ranchi. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751 To know about our editorial team click here
Disclaimer: This site is primarily intended for healthcare professionals. Any content/information on this website does not replace the advice of medical and/or health professionals and should not be construed as medical/diagnostic advice/endorsement or prescription. Use of this site is subject to our terms of use, privacy policy, advertisement policy. © 2020 Minerva Medical Treatment Pvt Ltd