# Amlodipine Besylate

NDC: 0615-8429
Generic name: Amlodipine besylate
Labeler / Manufacturer: NCS HealthCare of KY, LLC dba Vangard Labs
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20101020
Marketing ended: 20260930
FDA application: ANDA078925

## Active ingredients

- AMLODIPINE BESYLATE: 2.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0615-8429"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0615-8429
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=47f228e9-4a34-4d14-988d-b06af90124b9