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USFDA APPLICATION NUMBER - 12546 / DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| DIETHYLPROPION HYDROCHLORIDE(UNII: 19V2PL39NG) (DIETHYLPROPION - UNII:Q94YYU22B8) | DIETHYLPROPION HYDROCHLORIDE | 75mg |
Inactive Ingredients
| Ingredient Name | A-S Medication Solutions LLC | Actavis Pharma, Inc. | Bryant Ranch Prepack | NuCare Pharmaceuticals, Inc. | PD-Rx Pharmaceuticals, Inc. | Preferred Pharmaceuticals, Inc. |
|---|---|---|---|---|---|---|
| CARBOMER 934(Z135WT9208) | ||||||
| CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED)(Z135WT9208) | ||||||
| LACTOSE(J2B2A4N98G) | ||||||
| LACTOSE, UNSPECIFIED FORM(J2B2A4N98G) | ||||||
| MAGNESIUM STEARATE(70097M6I30) | ||||||
| MANNITOL(3OWL53L36A) | ||||||
| POVIDONE(FZ989GH94E) | ||||||
| POVIDONE, UNSPECIFIED(FZ989GH94E) | ||||||
| POVIDONES(FZ989GH94E) | ||||||
| STARCH, CORN(O8232NY3SJ) | ||||||
| TALC(7SEV7J4R1U) | ||||||
| TARTARIC ACID(W4888I119H) | ||||||
| ZINC STEARATE(H92E6QA4FV) |
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