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USFDA APPLICATION NUMBER - 12427 / DOSAGE - TABLET;ORAL - 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| benzphetamine hydrochloride(UNII: 43DWT87QT7) (benzphetamine - UNII:0M3S43XK27) | benzphetamine hydrochloride | 50mg |
Inactive Ingredients
| Ingredient Name | A-S Medication Solutions LLC | PD-Rx Pharmaceuticals, Inc. |
|---|---|---|
| calcium stearate(776XM7047L) | ||
| FD&C Red No. 3(PN2ZH5LOQY) | ||
| FD&C Yellow No. 6(H77VEI93A8) | ||
| lactose(J2B2A4N98G) | ||
| povidone(FZ989GH94E) | ||
| sorbitol(506T60A25R) | ||
| starch, corn(O8232NY3SJ) |
