# AMLODIPINE BESYLATE

NDC: 42806-055
Generic name: AMLODIPINE BESYLATE
Labeler / Manufacturer: Epic Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20110425

FDA application: ANDA078552

## 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:"42806-055"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42806-055
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=090f3e51-8129-4b5d-97f9-ab410e14df2d