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USFDA APPLICATION NUMBER - 17100 / DOSAGE - SUSPENSION/DROPS;OPHTHALMIC - 0.12%
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| prednisolone acetate(UNII: 8B2807733D) (prednisolone - UNII:9PHQ9Y1OLM) | prednisolone acetate | 1.2mg in 1 |
Inactive Ingredients
| Ingredient Name | Preferred Pharmaceuticals, Inc |
|---|---|
| benzalkonium chloride(F5UM2KM3W7) | |
| boric acid(R57ZHV85D4) | |
| edetate disodium(7FLD91C86K) | |
| HYPROMELLOSE, UNSPECIFIED(3NXW29V3WO) | |
| polysorbate 80(6OZP39ZG8H) | |
| sodium bisulfite(TZX5469Z6I) | |
| sodium chloride(451W47IQ8X) | |
| SODIUM CITRATE, UNSPECIFIED FORM(1Q73Q2JULR) | |
| water(059QF0KO0R) |
