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USFDA APPLICATION NUMBER - 20413 / DOSAGE - FOR SOLUTION;ORAL - 1MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| stavudine(UNII: BO9LE4QFZF) (stavudine - UNII:BO9LE4QFZF) | stavudine | 1mg in 1 | 40mg | 30mg | 20mg | 15mg |
Inactive Ingredients
| Ingredient Name | E.R. Squibb & Sons, L.L.C. |
|---|---|
| CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM(K679OBS311) | |
| cellulose, microcrystalline(OP1R32D61U) | |
| gelatin(2G86QN327L) | |
| GELATIN, UNSPECIFIED(2G86QN327L) | |
| lactose(J2B2A4N98G) | |
| LACTOSE, UNSPECIFIED FORM(J2B2A4N98G) | |
| magnesium stearate(70097M6I30) | |
| methylparaben(A2I8C7HI9T) | |
| MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | |
| propylparaben(Z8IX2SC1OH) | |
| sodium starch glycolate type A potato(5856J3G2A2) | |
| sucrose(C151H8M554) | |
| titanium dioxide(15FIX9V2JP) |
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