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$ API Ref.Price (USD/KG) : 53Xls

USFDA APPLICATION NUMBER - 19771 / DOSAGE - TABLET;ORAL - 200MG;30MG

Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
IBUPROFEN(UNII: WK2XYI10QM)
(IBUPROFEN - UNII:WK2XYI10QM)
IBUPROFEN200mg
PSEUDOEPHEDRINE HYDROCHLORIDE(UNII: 6V9V2RYJ8N)
(PSEUDOEPHEDRINE - UNII:7CUC9DDI9F)
PSEUDOEPHEDRINE HYDROCHLORIDE30mg

Inactive Ingredients

Ingredient Name
Haleon US Holdings LLC
CARNAUBA WAX(R12CBM0EIZ)
CROSCARMELLOSE SODIUM(M28OL1HH48)
DIACETYLATED MONOGLYCERIDES(5Z17386USF)
FERRIC OXIDE RED(1K09F3G675)
METHYLPARABEN(A2I8C7HI9T)
MICROCRYSTALLINE CELLULOSE(OP1R32D61U)
POVIDONE, UNSPECIFIED(FZ989GH94E)
PROPYLPARABEN(Z8IX2SC1OH)
SHELLAC(46N107B71O)
SILICON DIOXIDE(ETJ7Z6XBU4)
SODIUM BENZOATE(OJ245FE5EU)
SODIUM LAURYL SULFATE(368GB5141J)
STARCH, CORN(O8232NY3SJ)
STEARIC ACID(4ELV7Z65AP)
SUCROSE(C151H8M554)
TITANIUM DIOXIDE(15FIX9V2JP)