USFDA APPLICATION NUMBER - 20533 / DOSAGE - SOLUTION;INJECTION - 50MG/10ML (5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
ROPIVACAINE HYDROCHLORIDE MONOHYDRATE(UNII: V910P86109) (ROPIVACAINE - UNII:7IO5LYA57N) | ROPIVACAINE | 5mg in 1 |
Inactive Ingredients
Ingredient Name | APP Pharmaceuticals, LLC |
---|---|
HYDROCHLORIC ACID(QTT17582CB) | |
SODIUM CHLORIDE(451W47IQ8X) | |
SODIUM HYDROXIDE(55X04QC32I) |
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