Zydus receives final approval for Mycophenolate Mofetil Injection & Donepezil Hydrochloride Tablets

September 06, 2017 | Wednesday | News

Both the drugs will be manufactured at the group’s formulations manufacturing facility at Moraiya, Ahmedabad

Source: Pixabay

Source: Pixabay

Zydus Cadila has received the final approval from the USFDA to market Mycophenolate Mofetil for Injection USP, 500 mg/vial indicated for use in combination with other drugs i.e., cyclosporine and corticosteroids for the prophylaxis of organ rejection in patients receiving renal, hepatic or cardiac transplants.

It has also received an approval to market Donepezil Hydrochloride Tablets, in the strength of 23 mg. The drug is indicated for the treatment of dementia of the Alzheimer’s disease.

Both the drugs will be manufactured at the group’s formulations manufacturing facility at Moraiya, Ahmedabad.

Comments

× Your session has expired. Please click here to Sign-in or Sign-up

Have an Account?

Forgot your password?

First Name should not be empty!

Last Name should not be empty!

Email address should not be empty!

Show Password should not be empty!

Show Confirm Password should not be empty!

Newsletter

E-magazine

Biospectrum Infomercial

Bio Resource

I accept the terms & conditions & Privacy policy