
USFDA APPLICATION NUMBER - 20572 / DOSAGE - TABLET;ORAL - 500MG
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| SODIUM PHENYLBUTYRATE(UNII: NT6K61736T) (PHENYLBUTYRIC ACID - UNII:7WY7YBI87E) | SODIUM PHENYLBUTYRATE | 0.94g in 1 | 500mg |
Inactive Ingredients
| Ingredient Name | Hyperion Therapeutics, Inc. | Mikart, Inc. |
|---|---|---|
| CALCIUM STEARATE(776XM7047L) | ||
| CELLULOSE, MICROCRYSTALLINE(OP1R32D61U) | ||
| MAGNESIUM STEARATE(70097M6I30) | ||
| MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | ||
| SILICON DIOXIDE(ETJ7Z6XBU4) |