# Amlodipine Besylate

NDC: 65841-620
Generic name: Amlodipine Besylate
Labeler / Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20070921

FDA application: ANDA078226

## 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:"65841-620"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65841-620
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cacb3551-c579-41cb-bed6-4b4d8b0644fc