USFDA APPLICATION NUMBER - 20408 / DOSAGE - SOLUTION/DROPS;OPHTHALMIC - EQ 2% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
DORZOLAMIDE HYDROCHLORIDE(UNII: QZO5366EW7) (DORZOLAMIDE - UNII:9JDX055TW1) | DORZOLAMIDE | 20mg in 1 |
Inactive Ingredients
Ingredient Name | Merck Sharp & Dohme LLC | Prasco Laboratories |
---|---|---|
BENZALKONIUM CHLORIDE(F5UM2KM3W7) | ||
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)(S38J6RZN16) | ||
HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)(S38J6RZN16) | ||
MANNITOL(3OWL53L36A) | ||
sodium hydroxide(55X04QC32I) | ||
TRISODIUM CITRATE DIHYDRATE(B22547B95K) | ||
WATER(059QF0KO0R) |
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