USFDA APPLICATION NUMBER - 22396 / DOSAGE - SOLUTION;INTRAVENOUS - 37.5MG/ML (37.5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
DICLOFENAC SODIUM(UNII: QTG126297Q) (DICLOFENAC - UNII:144O8QL0L1) | DICLOFENAC SODIUM | 37.5mg in 1 |
Inactive Ingredients
Ingredient Name | Hospira, Inc. |
---|---|
HYDROCHLORIC ACID(QTT17582CB) | |
HYDROXYPROPYL BETADEX(1I96OHX6EK) | |
MONOTHIOGLYCEROL(AAO1P0WSXJ) | |
SODIUM HYDROXIDE(55X04QC32I) | |
WATER(059QF0KO0R) |