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USFDA APPLICATION NUMBER - 21199 / DOSAGE - SOLUTION/DROPS;OPHTHALMIC - 0.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 | 5mg in 1 |
Inactive Ingredients
| Ingredient Name | Vistakon Pharmaceuticals LLC |
|---|---|
| benzalkonium chloride(F5UM2KM3W7) | |
| hydrochloric acid(QTT17582CB) | |
| sodium chloride(451W47IQ8X) | |
| sodium hydroxide(55X04QC32I) | |
| water(059QF0KO0R) |
