 
				 
										
USFDA APPLICATION NUMBER - 20533 / DOSAGE - SOLUTION;INJECTION - 75MG/10ML (7.5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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) |