Application Information

This drug has been submitted to the FDA under the reference 021714/001.

Names and composition

"AMLODIPINE MALEATE; BENAZEPRIL HYDROCHLORIDE" is the commercial name of a drug composed of AMLODIPINE MALEATE and BENAZEPRIL HYDROCHLORIDE.

Forms

ApplId/ProductId Drug name Active ingredient Form Strenght
021714/001 AMLODIPINE MALEATE; BENAZEPRIL HYDROCHLORIDE AMLODIPINE MALEATE; BENAZEPRIL HYDROCHLORIDE CAPSULE/ ORAL 2.5MG and 10MG
021714/002 AMLODIPINE MALEATE; BENAZEPRIL HYDROCHLORIDE AMLODIPINE MALEATE; BENAZEPRIL HYDROCHLORIDE CAPSULE/ ORAL 5MG and 10MG
021714/003 AMLODIPINE MALEATE; BENAZEPRIL HYDROCHLORIDE AMLODIPINE MALEATE; BENAZEPRIL HYDROCHLORIDE CAPSULE/ ORAL 5MG and 20MG
021714/004 AMLODIPINE MALEATE; BENAZEPRIL HYDROCHLORIDE AMLODIPINE MALEATE; BENAZEPRIL HYDROCHLORIDE CAPSULE/ ORAL 10MG and 20MG

Similar Active Ingredient

ApplId/ProductId Drug name Active ingredient Form Strenght
021714/001 AMLODIPINE MALEATE; BENAZEPRIL HYDROCHLORIDE AMLODIPINE MALEATE; BENAZEPRIL HYDROCHLORIDE CAPSULE/ ORAL 2.5MG and 10MG
021714/002 AMLODIPINE MALEATE; BENAZEPRIL HYDROCHLORIDE AMLODIPINE MALEATE; BENAZEPRIL HYDROCHLORIDE CAPSULE/ ORAL 5MG and 10MG
021714/003 AMLODIPINE MALEATE; BENAZEPRIL HYDROCHLORIDE AMLODIPINE MALEATE; BENAZEPRIL HYDROCHLORIDE CAPSULE/ ORAL 5MG and 20MG
021714/004 AMLODIPINE MALEATE; BENAZEPRIL HYDROCHLORIDE AMLODIPINE MALEATE; BENAZEPRIL HYDROCHLORIDE CAPSULE/ ORAL 10MG and 20MG

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