USFDA APPLICATION NUMBER - 19219 / DOSAGE - SOLUTION/DROPS;OPHTHALMIC - 0.5%
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
levobunolol hydrochloride(UNII: O90S49LDHH) (levobunolol - UNII:G6317AOI7K) | levobunolol hydrochloride | 5mg in 1 | 2.5mg in 1 |
Inactive Ingredients
Ingredient Name | Allergan, Inc. | Pacific Pharma, Inc. | Sandoz Inc |
---|---|---|---|
BENZALKONIUM CHLORIDE(F5UM2KM3W7) | |||
EDETATE DISODIUM(7FLD91C86K) | |||
HYDROCHLORIC ACID(QTT17582CB) | |||
POLYVINYL ALCOHOL(532B59J990) | |||
POLYVINYL ALCOHOL, UNSPECIFIED(532B59J990) | |||
potassium phosphate, monobasic(4J9FJ0HL51) | |||
sodium chloride(451W47IQ8X) | |||
SODIUM HYDROXIDE(55X04QC32I) | |||
SODIUM METABISULFITE(4VON5FNS3C) | |||
SODIUM PHOSPHATE, DIBASIC(GR686LBA74) | |||
water(059QF0KO0R) |
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