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 name | KATERZIA |
|---|---|
| Active ingredients | AMLODIPINE BENZOATE |
| Application number | NDA211340 |
| Sponsor | AZURITY |
| Dosage form | SUSPENSION |
| Route | ORAL |
| Marketing status | Prescription |
| Products in application | 1 |
| First approval date | 20190708 |
| Source | openFDA Drugs@FDA |
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