Zydus Cadila gets USFDA approval for arthritis drug
Zydus Cadila has received the final approval from the United States Food and Drug Administration (USFDA) to market Piroxicam Capsules USP in the strengths of 10 mg and 20 mg, the company said in a BSE filing
New Delhi: Zydus Cadila has received final approval from the US health regulator for Piroxicam Capsules, used for the treatment of osteoarthritis and rheumatoid arthritis.
Zydus Cadila has received the final approval from the United States Food and Drug Administration (USFDA) to market Piroxicam Capsules USP in the strengths of 10 mg and 20 mg, the company said in a BSE filing.
Zydus Cadila said the drug will be produced at the group's manufacturing facility at SEZ, Ahmedabad.
The group has more than 209 approvals, and so far filed over 330 abbreviated new drug applications (ANDAs) since it started filings in 2003-04.
abbreviated new drug applicationsAhmedabadapprovalarthritis drugfinal approvalmanufacturing facilitymarketOsteoarthritisPiroxicam capsulesrheumatoid arthritisUnited States Food and Drug AdministrationUSFDAZydus Cadila
Source : PTINext Story
NO DATA FOUND
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