USFDA APPLICATION NUMBER - 22108 / DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 522MG
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
BUPROPION HYDROBROMIDE(UNII: E70G3G5863) (BUPROPION - UNII:01ZG3TPX31) | BUPROPION HYDROBROMIDE | 522mg | 348mg | 174mg |
Inactive Ingredients
Ingredient Name | sanofi-aventis U.S. LLC |
---|---|
CARNAUBA WAX(R12CBM0EIZ) | |
DIBUTYL SEBACATE(4W5IH7FLNY) | |
ETHYLCELLULOSE (100 MPA.S)(47MLB0F1MV) | |
GLYCERYL DIBEHENATE(R8WTH25YS2) | |
POLYETHYLENE GLYCOLS(3WJQ0SDW1A) | |
POLYVINYL ALCOHOL(532B59J990) | |
POVIDONES(FZ989GH94E) |
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