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USFDA APPLICATION NUMBER - 19898 / DOSAGE - TABLET;ORAL - 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| pravastatin sodium(UNII: 3M8608UQ61) (pravastatin - UNII:KXO2KT9N0G) | pravastatin sodium | 80mg | 40mg | 20mg |
Inactive Ingredients
| Ingredient Name | E.R. Squibb & Sons, L.L.C. |
|---|---|
| aluminum hydroxide(5QB0T2IUN0) | |
| croscarmellose sodium(M28OL1HH48) | |
| D&C Yellow No. 10(35SW5USQ3G) | |
| FD&C Blue No. 1(H3R47K3TBD) | |
| ferric oxide yellow(EX438O2MRT) | |
| LACTOSE, UNSPECIFIED FORM(J2B2A4N98G) | |
| magnesium oxide(3A3U0GI71G) | |
| magnesium stearate(70097M6I30) | |
| MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | |
| POVIDONE, UNSPECIFIED(FZ989GH94E) |
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