USFDA APPLICATION NUMBER - 21537 / DOSAGE - SUSPENSION/DROPS;OTIC - 0.3%;0.1%
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
Ciprofloxacin Hydrochloride(UNII: 4BA73M5E37) (Ciprofloxacin - UNII:5E8K9I0O4U) | Ciprofloxacin | 3mg in 1 |
Dexamethasone(UNII: 7S5I7G3JQL) (Dexamethasone - UNII:7S5I7G3JQL) | Dexamethasone | 1mg in 1 |
Inactive Ingredients
Ingredient Name | Alcon Laboratories, Inc. | ARMAS PHARMACEUTICALS INC. | Clinical Solutions Wholesale | NuCare Pharmaceuticals,Inc. |
---|---|---|---|---|
Acetic Acid(Q40Q9N063P) | ||||
BENZALKONIUM CHLORIDE(F5UM2KM3W7) | ||||
BORIC ACID(R57ZHV85D4) | ||||
EDETATE DISODIUM(7FLD91C86K) | ||||
Hydrochloric Acid(QTT17582CB) | ||||
HYDROXYETHYL CELLULOSE (1500 MPA.S AT 1%)(L605B5892V) | ||||
HYDROXYETHYL CELLULOSE, UNSPECIFIED(T4V6TWG28D) | ||||
SODIUM ACETATE(4550K0SC9B) | ||||
SODIUM CHLORIDE(451W47IQ8X) | ||||
SODIUM HYDROXIDE(55X04QC32I) | ||||
Tyloxapol(Y27PUL9H56) | ||||
WATER(059QF0KO0R) |
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