USFDA APPLICATION NUMBER - 21202 / DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 | 750mg | 500mg | 1000mg | 850mg | 500mg |
Inactive Ingredients
Ingredient Name | Bristol-Myers Squibb Company |
---|---|
carboxymethylcellulose sodium(K679OBS311) | |
cellulose, microcrystalline(OP1R32D61U) | |
hypromelloses(3NXW29V3WO) | |
magnesium stearate(70097M6I30) | |
polyethylene glycol 400(B697894SGQ) | |
polyethylene glycol 8000(Q662QK8M3B) | |
POVIDONE, UNSPECIFIED(FZ989GH94E) |
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