USFDA APPLICATION NUMBER - 21574 / DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
METFORMIN HYDROCHLORIDE(UNII: 786Z46389E) (METFORMIN - UNII:9100L32L2N) | METFORMIN HYDROCHLORIDE | 1000mg |
Inactive Ingredients
Ingredient Name | Lake Erie Medical DBA Quality Care Products LLC | Bristol-Myers Squibb Company |
---|---|---|
CANDELILLA WAX(WL0328HX19) | ||
carboxymethylcellulose sodium(K679OBS311) | ||
CELLULOSE ACETATE(3J2P07GVB6) | ||
cellulose, microcrystalline(OP1R32D61U) | ||
FERROSOFERRIC OXIDE(XM0M87F357) | ||
hypromelloses(3NXW29V3WO) | ||
magnesium stearate(70097M6I30) | ||
polyethylene glycol 400(B697894SGQ) | ||
POLYETHYLENE GLYCOL 8000(Q662QK8M3B) | ||
POLYSORBATE 80(6OZP39ZG8H) | ||
POVIDONE(FZ989GH94E) | ||
POVIDONE, UNSPECIFIED(FZ989GH94E) | ||
SODIUM LAURYL SULFATE(368GB5141J) | ||
TITANIUM DIOXIDE(15FIX9V2JP) | ||
TRIACETIN(XHX3C3X673) |
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