# Katerzia

NDC: 52652-5001
Generic name: Amlodipine
Labeler / Manufacturer: Azurity Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20190815

FDA application: NDA211340

## Active ingredients

- AMLODIPINE BENZOATE: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"52652-5001"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=52652-5001
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=df673a4d-acb8-444c-a472-c87ab8cbd366