Application Information

This drug has been submitted to the FDA under the reference 087835/001.

Names and composition

"OXTRIPHYLLINE" is the commercial name of a drug composed of OXTRIPHYLLINE.

Forms

ApplId/ProductId Drug name Active ingredient Form Strenght
087835/001 OXTRIPHYLLINE OXTRIPHYLLINE TABLET, DELAYED RELEASE/ORAL 200MG
087866/001 OXTRIPHYLLINE OXTRIPHYLLINE TABLET, DELAYED RELEASE/ORAL 100MG
088243/001 OXTRIPHYLLINE OXTRIPHYLLINE SOLUTION/ORAL 100MG per 5ML

Similar Active Ingredient

ApplId/ProductId Drug name Active ingredient Form Strenght
009268/003 CHOLEDYL OXTRIPHYLLINE TABLET, DELAYED RELEASE/ORAL 100MG
009268/007 CHOLEDYL OXTRIPHYLLINE TABLET, DELAYED RELEASE/ORAL 200MG
009268/011 CHOLEDYL OXTRIPHYLLINE SYRUP/ORAL 50MG per 5ML
009268/012 CHOLEDYL OXTRIPHYLLINE SOLUTION/ORAL 100MG per 5ML
086742/001 CHOLEDYL SA OXTRIPHYLLINE TABLET, EXTENDED RELEASE/ORAL 600MG
087835/001 OXTRIPHYLLINE OXTRIPHYLLINE TABLET, DELAYED RELEASE/ORAL 200MG
087863/001 CHOLEDYL SA OXTRIPHYLLINE TABLET, EXTENDED RELEASE/ORAL 400MG
087866/001 OXTRIPHYLLINE OXTRIPHYLLINE TABLET, DELAYED RELEASE/ORAL 100MG
088242/001 OXTRIPHYLLINE PEDIATRIC OXTRIPHYLLINE SYRUP/ORAL 50MG per 5ML
088243/001 OXTRIPHYLLINE OXTRIPHYLLINE SOLUTION/ORAL 100MG per 5ML

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