
USFDA APPLICATION NUMBER - 21571 / DOSAGE - SOLUTION/DROPS;OPHTHALMIC - 1.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| levofloxacin(UNII: 6GNT3Y5LMF) (levofloxacin anhydrous - UNII:RIX4E89Y14) | levofloxacin anhydrous | 15mg in 1 |
Inactive Ingredients
| Ingredient Name | Vistakon Pharmaceuticals LLC |
|---|---|
| glycerin(PDC6A3C0OX) | |
| hydrochloric acid(QTT17582CB) | |
| sodium hydroxide(55X04QC32I) | |
| water(059QF0KO0R) |