
USFDA APPLICATION NUMBER - 20357 / DOSAGE - TABLET;ORAL - 850MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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) |