USFDA APPLICATION NUMBER - 212595 / DOSAGE - FOR SUSPENSION, EXTENDED RELEASE;ORAL - 500MG/5ML
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
METFORMIN HYDROCHLORIDE(UNII: 786Z46389E) (METFORMIN - UNII:9100L32L2N) | METFORMIN HYDROCHLORIDE | 500mg in 5 |
Inactive Ingredients
Ingredient Name | Sun Pharmaceutical Industries Inc. |
---|---|
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM(K679OBS311) | |
DIBUTYL SEBACATE(4W5IH7FLNY) | |
ETHYLCELLULOSE, UNSPECIFIED(7Z8S9VYZ4B) | |
GLYCERIN(PDC6A3C0OX) | |
HYPROMELLOSE, UNSPECIFIED(3NXW29V3WO) | |
MAGNESIUM STEARATE(70097M6I30) | |
METHYLPARABEN(A2I8C7HI9T) | |
MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | |
PROPYLENE GLYCOL, (S)-(942194N4TD) | |
PROPYLPARABEN(Z8IX2SC1OH) | |
SILICON DIOXIDE(ETJ7Z6XBU4) | |
SUCRALOSE(96K6UQ3ZD4) | |
XANTHAN GUM(TTV12P4NEE) | |
XYLITOL(VCQ006KQ1E) |
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