USFDA APPLICATION NUMBER - 20357 / DOSAGE - TABLET;ORAL - 750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 | 500mg |
Inactive Ingredients
Ingredient Name | Bristol-Myers Squibb Company | PD-Rx Pharmaceuticals, Inc. |
---|---|---|
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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