USFDA APPLICATION NUMBER - 200153 / DOSAGE - TABLET;ORAL - EQ 40MG BASE;10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
ATORVASTATIN CALCIUM TRIHYDRATE(UNII: 48A5M73Z4Q) (ATORVASTATIN - UNII:A0JWA85V8F) | ATORVASTATIN | 80mg | 40mg | 20mg | 10mg |
EZETIMIBE(UNII: EOR26LQQ24) (EZETIMIBE - UNII:EOR26LQQ24) | EZETIMIBE | 10mg | 10mg | 10mg | 10mg |
Inactive Ingredients
Ingredient Name | Merck Sharp & Dohme Corp. |
---|---|
ANHYDROUS LACTOSE(3SY5LH9PMK) | |
CARNAUBA WAX(R12CBM0EIZ) | |
CROSCARMELLOSE SODIUM(M28OL1HH48) | |
HYDROXYPROPYL CELLULOSE (1200000 MW)(RFW2ET671P) | |
HYPROMELLOSE 2910 (6 MPA.S)(0WZ8WG20P6) | |
LACTOSE MONOHYDRATE(EWQ57Q8I5X) | |
MAGNESIUM STEARATE(70097M6I30) | |
MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | |
POVIDONE K29/32(390RMW2PEQ) | |
SODIUM BICARBONATE(8MDF5V39QO) | |
SODIUM LAURYL SULFATE(368GB5141J) | |
TITANIUM DIOXIDE(15FIX9V2JP) |
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