Drug profile · INN
cyclosporine
RESTASIS
- US status
- approved
- Patents linked
- 8
- News articles
- 0
Quick answer
cyclosporine (RESTASIS) is an FDA-listed pharmaceutical active ingredient. Associated with Amneal Pharma Europe Ltd. Route of administration: ophthalmic. Current US regulatory status: approved.
Key facts
Related patents
Search patents →-
US 12409206
Use of cyclosporine analogues for treating fibrosis
granted -
US 10472394
Cyclosporine analogue mixtures and their use as immunomodulating agents
granted -
US 9765119
Cyclosporine analogue mixtures and their use as immunomodulating agents
granted -
US 7521421
Deuterated cyclosporine analogs and methods of making the same
granted -
US 7332472
Cyclosporine analogue mixtures and their use as immunomodulating agents
granted -
US 6998385
Cyclosporine analogue mixtures and their use as immunomodulating agents
expired -
US 6686454
Antibodies to specific regions of cyclosporine related compounds
expired -
US 6613739
Deuterated cyclosporine analogs and their use as immunomodulating agents
expired
Frequently asked questions
What is cyclosporine?
cyclosporine (RESTASIS) is an FDA-listed pharmaceutical active ingredient. Associated with Amneal Pharma Europe Ltd. Route of administration: ophthalmic. Current US regulatory status: approved.
What is the brand name for cyclosporine?
RESTASIS is a marketed brand name for cyclosporine. Check FDA Drugs@FDA for the current US label holder and prescribing information.
What is the US approval status of cyclosporine?
cyclosporine has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.