Orange Book product
KETOTIFEN FUMARATE EQ 0.025% BASE
Orange Book ANDA 077958 · SENTISS AG · Over the counter
Key facts
| Proprietary name | KETOTIFEN FUMARATE |
|---|---|
| Active ingredients | KETOTIFEN FUMARATE |
| Strength | EQ 0.025% BASE |
| Dosage form | SOLUTION/DROPS |
| Route | OPHTHALMIC |
| Application | ANDA077958 |
| Applicant holder | SENTISS AG |
| Marketing status | Over the counter |
| Reference listed drug (RLD) | No |
| Reference standard (RS) | No |
| Approval date | Jul 26, 2007 |
At a glance
- 1–9 Marketed products with the same ingredient, strength and form
- 1–9 Products in this application
- No Reference listed drug
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Orange Book products
The FDA Orange Book lists approved drug products with their therapeutic equivalence (TE) codes, reference listed drugs and marketing status. Products approved before 1982 show an approval date of Jan 1, 1982.