USFDA APPLICATION NUMBER - 22246 / DOSAGE - TABLET, ORALLY DISINTEGRATING;ORAL - EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
METOCLOPRAMIDE HYDROCHLORIDE(UNII: W1792A2RVD) (METOCLOPRAMIDE - UNII:L4YEB44I46) | METOCLOPRAMIDE | 5mg | 10mg |
Inactive Ingredients
Ingredient Name | Salix Pharmaceuticals, Inc. |
---|---|
ACESULFAME POTASSIUM(23OV73Q5G9) | |
GELATIN(2G86QN327L) | |
MANNITOL(3OWL53L36A) | |
SODIUM CHLORIDE(451W47IQ8X) | |
SODIUM HYDROXIDE(55X04QC32I) |
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