USFDA APPLICATION NUMBER - 21909 / DOSAGE - TABLET, ORALLY DISINTEGRATING;ORAL - 30MG
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
fexofenadine hydrochloride(UNII: 2S068B75ZU) (fexofenadine - UNII:E6582LOH6V) | fexofenadine hydrochloride | 6mg in 1 | 180mg | 60mg | 30mg | 30mg |
Inactive Ingredients
Ingredient Name | Chattem, Inc. | sanofi-aventis U.S. LLC |
---|---|---|
anhydrous citric acid(XF417D3PSL) | ||
aspartame(Z0H242BBR1) | ||
butylparaben(3QPI1U3FV8) | ||
cellulose acetate(3J2P07GVB6) | ||
cellulose, microcrystalline(OP1R32D61U) | ||
croscarmellose sodium(M28OL1HH48) | ||
crospovidone(68401960MK) | ||
edetate disodium(7FLD91C86K) | ||
hypromelloses(3NXW29V3WO) | ||
magnesium stearate(70097M6I30) | ||
MANNITOL(3OWL53L36A) | ||
poloxamer 407(TUF2IVW3M2) | ||
polyethylene glycols(3WJQ0SDW1A) | ||
povidone K30(U725QWY32X) | ||
povidone(FZ989GH94E) | ||
POVIDONES(FZ989GH94E) | ||
propylene glycol(6DC9Q167V3) | ||
propylparaben(Z8IX2SC1OH) | ||
silicon dioxide(ETJ7Z6XBU4) | ||
sodium bicarbonate(8MDF5V39QO) | ||
sodium chloride(451W47IQ8X) | ||
sodium phosphate, dibasic, heptahydrate(70WT22SF4B) | ||
sodium phosphate, monobasic, monohydrate(593YOG76RN) | ||
SODIUM STARCH GLYCOLATE TYPE A POTATO(5856J3G2A2) | ||
sucrose(C151H8M554) | ||
titanium dioxide(15FIX9V2JP) | ||
water(059QF0KO0R) | ||
xanthan gum(TTV12P4NEE) | ||
xylitol(VCQ006KQ1E) |
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