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KATERZIA (AMLODIPINE BENZOATE) — FDA Approval NDA211340 (AZURITY)

KATERZIA (AMLODIPINE BENZOATE) — FDA Approval NDA211340 (AZURITY) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: KATERZIA; Active ingredients: AMLODIPINE BENZOATE; Application number: NDA211340.

Brand nameKATERZIA
Active ingredientsAMLODIPINE BENZOATE
Application numberNDA211340
SponsorAZURITY
Dosage formSUSPENSION
RouteORAL
Marketing statusPrescription
Products in application1
First approval date20190708
SourceopenFDA Drugs@FDA

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