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Drug Product Composition: Benzphetamine

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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NUMBER - 12427 / DOSAGE - TABLET;ORAL - 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 hydrochloride50mg

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)