USFDA APPLICATION NUMBER - 22331 / DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 0.1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
CLONIDINE HYDROCHLORIDE(UNII: W76I6XXF06) (CLONIDINE - UNII:MN3L5RMN02) | CLONIDINE HYDROCHLORIDE | 0.1mg |
Inactive Ingredients
Ingredient Name | Concordia Pharmaceuticals Inc. | Prasco Laboratories |
---|---|---|
HYPROMELLOSE 2208 (15000 MPA.S)(Z78RG6M2N2) | ||
LACTOSE MONOHYDRATE(EWQ57Q8I5X) | ||
MAGNESIUM STEARATE(70097M6I30) | ||
SILICON DIOXIDE(ETJ7Z6XBU4) | ||
SODIUM LAURYL SULFATE(368GB5141J) | ||
STARCH, CORN(O8232NY3SJ) |
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