
USFDA APPLICATION NUMBER - 16801 / DOSAGE - INJECTABLE;INJECTION - 20% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| LIDOCAINE HYDROCHLORIDE(UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) | LIDOCAINE HYDROCHLORIDE | 20mg in 1 |
Inactive Ingredients
| Ingredient Name | APP Pharmaceuticals, LLC |
|---|---|
| HYDROCHLORIC ACID(QTT17582CB) | |
| SODIUM CHLORIDE(451W47IQ8X) | |
| SODIUM HYDROXIDE(55X04QC32I) |