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USFDA APPLICATION NUMBER - 87801 / DOSAGE - TABLET;ORAL - 2.5MG
| 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 | Bryant Ranch Prepack | Preferred Pharmaceuticals, Inc. | Safecor Health, LLC | Denton Pharma, Inc. DBA Northwind Pharmaceuticals | GeneYork Pharmaceuticals Group LLC | Lannett Company, Inc. | NCS HealthCare of KY, Inc dba Vangard Labs | Northwind Pharmaceuticals | Redpharm Drug, Inc. | REMEDYREPACK INC. | A-S Medication Solutions | Preferred Pharmaceuticals Inc. | Proficient Rx LP | ASE Direct, Inc. | NuCare Pharmaceuticals,Inc. | St. Mary's Medical Park Pharmacy | Unit Dose Services |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Aluminum Oxide(LMI26O6933) | |||||||||||||||||
| CELLULOSE, MICROCRYSTALLINE(OP1R32D61U) | |||||||||||||||||
| CROSCARMELLOSE SODIUM(M28OL1HH48) | |||||||||||||||||
| Fd&c Yellow No. 6(H77VEI93A8) | |||||||||||||||||
| 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, Potato(8I089SAH3T) | |||||||||||||||||
| STEARIC ACID(4ELV7Z65AP) |
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