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21571 / DOSAGE - SOLUTION/DROPS;OPHTHALMIC - 1.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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) |
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