USFDA APPLICATION NUMBER - 17469 / DOSAGE - SUSPENSION/DROPS;OPHTHALMIC - 1%
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
PREDNISOLONE ACETATE(UNII: 8B2807733D) (PREDNISOLONE - UNII:9PHQ9Y1OLM) | PREDNISOLONE ACETATE | 10mg in 1 |
Inactive Ingredients
Ingredient Name | A-S Medication Solutions LLC | Alcon Laboratories, Inc. | Clinical Solutions Wholesale | NuCare Pharmaceuticals,Inc. | Preferred Pharmaceuticals, Inc. | REMEDYREPACK INC. |
---|---|---|---|---|---|---|
benzalkonium chloride(F5UM2KM3W7) | ||||||
BORIC ACID(R57ZHV85D4) | ||||||
CITRIC ACID MONOHYDRATE(2968PHW8QP) | ||||||
edetate disodium(7FLD91C86K) | ||||||
GLYCERIN(PDC6A3C0OX) | ||||||
HYPROMELLOSES(3NXW29V3WO) | ||||||
polysorbate 80(6OZP39ZG8H) | ||||||
sodium bisulfite(TZX5469Z6I) | ||||||
SODIUM CHLORIDE(451W47IQ8X) | ||||||
SODIUM CITRATE(1Q73Q2JULR) | ||||||
SODIUM HYDROXIDE(55X04QC32I) | ||||||
SODIUM PHOSPHATE, DIBASIC(GR686LBA74) | ||||||
WATER(059QF0KO0R) |
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