
USFDA APPLICATION NUMBER - 19527 / DOSAGE - FOR SUSPENSION;ORAL - 40MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| FAMOTIDINE(UNII: 5QZO15J2Z8) (FAMOTIDINE - UNII:5QZO15J2Z8) | FAMOTIDINE | 40mg in 5 |
Inactive Ingredients
| Ingredient Name | Salix Pharmaceuticals, Inc |
|---|---|
| CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM(K679OBS311) | |
| CITRIC ACID MONOHYDRATE(2968PHW8QP) | |
| METHYLPARABEN SODIUM(CR6K9C2NHK) | |
| MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | |
| PROPYLPARABEN SODIUM(625NNB0G9N) | |
| SODIUM BENZOATE(OJ245FE5EU) | |
| SUCROSE(C151H8M554) | |
| XANTHAN GUM(TTV12P4NEE) |