
USFDA APPLICATION NUMBER - 21345 / DOSAGE - INJECTABLE;SUBCUTANEOUS - 5MG/0.4ML
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| FONDAPARINUX SODIUM(UNII: X0Q6N9USOZ) (FONDAPARINUX - UNII:J177FOW5JL) | FONDAPARINUX SODIUM | 2.5mg in 0.5 | 5mg in 0.4 | 7.5mg in 0.6 | 10mg in 0.8 |
Inactive Ingredients
| Ingredient Name | Apotex Corp. | GlaxoSmithKline LLC | Mylan Institutional LLC |
|---|---|---|---|
| SODIUM CHLORIDE(451W47IQ8X) | |||
| WATER(059QF0KO0R) |