USFDA APPLICATION NUMBER - 19814 / DOSAGE - SOLUTION/DROPS;OPHTHALMIC - 0.25% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
levobunolol hydrochloride(UNII: O90S49LDHH) (levobunolol - UNII:G6317AOI7K) | levobunolol hydrochloride | 5mg in 1 | 2.5mg in 1 |
Inactive Ingredients
Ingredient Name | Pacific Pharma, Inc. |
---|---|
benzalkonium chloride(F5UM2KM3W7) | |
edetate disodium(7FLD91C86K) | |
hydrochloric acid(QTT17582CB) | |
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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