USFDA APPLICATION NUMBER - 50725 / DOSAGE - FOR SUSPENSION;ORAL - 400MG/5ML;EQ 57MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
AMOXICILLIN(UNII: 804826J2HU) (AMOXICILLIN ANHYDROUS - UNII:9EM05410Q9) | AMOXICILLIN ANHYDROUS | 400mg in 5 |
CLAVULANATE POTASSIUM(UNII: Q42OMW3AT8) (CLAVULANIC ACID - UNII:23521W1S24) | CLAVULANIC ACID | 57mg in 5 |
Inactive Ingredients
Ingredient Name | Preferred Pharmaceuticals, Inc. | REMEDYREPACK INC. |
---|---|---|
ASPARTAME(Z0H242BBR1) | ||
HYPROMELLOSE, UNSPECIFIED(3NXW29V3WO) | ||
HYPROMELLOSES(3NXW29V3WO) | ||
MANNITOL(3OWL53L36A) | ||
SACCHARIN SODIUM(SB8ZUX40TY) | ||
SILICON DIOXIDE(ETJ7Z6XBU4) | ||
XANTHAN GUM(TTV12P4NEE) |