Application Information

This drug has been submitted to the FDA under the reference 075706/001.

Names and composition

"LORATADINE AND PSEUDOEPHEDRINE SULFATE" is the commercial name of a drug composed of LORATADINE and PSEUDOEPHEDRINE SULFATE.

Forms

ApplId/ProductId Drug name Active ingredient Form Strenght
075706/001 LORATADINE AND PSEUDOEPHEDRINE SULFATE LORATADINE; PSEUDOEPHEDRINE SULFATE TABLET, EXTENDED RELEASE/ORAL 10MG and 240MG
075989/001 LORATADINE AND PSEUDOEPHEDRINE SULFATE LORATADINE; PSEUDOEPHEDRINE SULFATE TABLET, EXTENDED RELEASE/ORAL 10MG and 240MG
076050/001 LORATADINE AND PSEUDOEPHEDRINE SULFATE LORATADINE; PSEUDOEPHEDRINE SULFATE TABLET, EXTENDED RELEASE/ORAL 5MG and 120MG
076208/001 LORATADINE AND PSEUDOEPHEDRINE SULFATE LORATADINE; PSEUDOEPHEDRINE SULFATE TABLET, EXTENDED RELEASE/ORAL 5MG and 120MG
076557/001 LORATADINE AND PSEUDOEPHEDRINE SULFATE LORATADINE; PSEUDOEPHEDRINE SULFATE TABLET, EXTENDED RELEASE/ORAL 10MG and 240MG

Similar Active Ingredient

ApplId/ProductId Drug name Active ingredient Form Strenght
019670/002 CLARITIN-D LORATADINE; PSEUDOEPHEDRINE SULFATE TABLET, EXTENDED RELEASE/ORAL 5MG and 120MG
020470/002 CLARITIN-D 24 HOUR LORATADINE; PSEUDOEPHEDRINE SULFATE TABLET, EXTENDED RELEASE/ORAL 10MG and 240MG
075706/001 LORATADINE AND PSEUDOEPHEDRINE SULFATE LORATADINE; PSEUDOEPHEDRINE SULFATE TABLET, EXTENDED RELEASE/ORAL 10MG and 240MG
075989/001 LORATADINE AND PSEUDOEPHEDRINE SULFATE LORATADINE; PSEUDOEPHEDRINE SULFATE TABLET, EXTENDED RELEASE/ORAL 10MG and 240MG
076050/001 LORATADINE AND PSEUDOEPHEDRINE SULFATE LORATADINE; PSEUDOEPHEDRINE SULFATE TABLET, EXTENDED RELEASE/ORAL 5MG and 120MG
076208/001 LORATADINE AND PSEUDOEPHEDRINE SULFATE LORATADINE; PSEUDOEPHEDRINE SULFATE TABLET, EXTENDED RELEASE/ORAL 5MG and 120MG
076557/001 LORATADINE AND PSEUDOEPHEDRINE SULFATE LORATADINE; PSEUDOEPHEDRINE SULFATE TABLET, EXTENDED RELEASE/ORAL 10MG and 240MG

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