
USFDA APPLICATION NUMBER - 21223 / DOSAGE - INJECTABLE;INTRAVENOUS - EQ 4MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| ZOLEDRONIC ACID(UNII: 6XC1PAD3KF) (ZOLEDRONIC ACID ANHYDROUS - UNII:70HZ18PH24) | ZOLEDRONIC ACID ANHYDROUS | 4mg in 100 | 4mg in 5 |
Inactive Ingredients
| Ingredient Name | Novartis Pharmaceuticals Corporation |
|---|---|
| MANNITOL(3OWL53L36A) | |
| SODIUM CITRATE(1Q73Q2JULR) | |
| WATER(059QF0KO0R) |