USFDA APPLICATION NUMBER - 87800 / DOSAGE - TABLET;ORAL - 1MG
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
PREDNISONE(UNII: VB0R961HZT) (PREDNISONE - UNII:VB0R961HZT) | PREDNISONE | 20mg | 2.5mg | 1mg |
Inactive Ingredients
Ingredient Name | NCS HealthCare of KY, Inc dba Vangard Labs | Bryant Ranch Prepack | GeneYork Pharmaceuticals Group LLC | Lannett Company, Inc. | Northwind Pharmaceuticals | REMEDYREPACK INC. |
---|---|---|---|---|---|---|
CELLULOSE, MICROCRYSTALLINE(OP1R32D61U) | ||||||
LACTOSE MONOHYDRATE(EWQ57Q8I5X) | ||||||
LACTOSE(J2B2A4N98G) | ||||||
MAGNESIUM STEARATE(70097M6I30) | ||||||
MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | ||||||
SILICON DIOXIDE(ETJ7Z6XBU4) | ||||||
SODIUM GLYCOLATE(B75E535IMI) | ||||||
SODIUM LAURYL SULFATE(368GB5141J) | ||||||
SODIUM STARCH GLYCOLATE TYPE A POTATO(5856J3G2A2) | ||||||
STARCH, CORN(O8232NY3SJ) | ||||||
STARCH, PREGELATINIZED CORN(O8232NY3SJ) | ||||||
STEARIC ACID(4ELV7Z65AP) |
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