
USFDA APPLICATION NUMBER - 20313 / DOSAGE - SPRAY, METERED;NASAL - 200 IU/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| CALCITONIN SALMON(UNII: 7SFC6U2VI5) (CALCITONIN SALMON - UNII:7SFC6U2VI5) | CALCITONIN SALMON | 200[iU] |
Inactive Ingredients
| Ingredient Name | Novartis Pharmaceuticals Corporation | Sandoz Inc | Upsher-Smith Laboratories, Inc. |
|---|---|---|---|
| BENZALKONIUM CHLORIDE(F5UM2KM3W7) | |||
| benzyl alcohol(LKG8494WBH) | |||
| citric acid monohydrate(2968PHW8QP) | |||
| HYDROCHLORIC ACID(QTT17582CB) | |||
| phenylethyl alcohol(ML9LGA7468) | |||
| polysorbate 80(6OZP39ZG8H) | |||
| SODIUM CHLORIDE(451W47IQ8X) | |||
| sodium hydroxide(55X04QC32I) | |||
| WATER(059QF0KO0R) |