
USFDA APPLICATION NUMBER - 20379 / DOSAGE - INJECTABLE;INJECTION - 0.005MG/VIAL
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| ALPROSTADIL(UNII: F5TD010360) (ALPROSTADIL - UNII:F5TD010360) | ALPROSTADIL | 41.1ug in 1 | 20.5ug in 1 |
Inactive Ingredients
| Ingredient Name | Pharmacia & Upjohn Company LLC |
|---|---|
| BENZYL ALCOHOL(LKG8494WBH) | |
| HYDROCHLORIC ACID(QTT17582CB) | |
| LACTOSE, UNSPECIFIED FORM(J2B2A4N98G) | |
| SODIUM CITRATE, UNSPECIFIED FORM(1Q73Q2JULR) | |
| SODIUM HYDROXIDE(55X04QC32I) | |
| WATER(059QF0KO0R) |