# AMLODIPINE BESYLATE 2.5 mg

NDC: 69584-021
Generic name: AMLODIPINE BESYLATE
Labeler / Manufacturer: Oxford Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20211001

FDA application: ANDA078414

## 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:"69584-021"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69584-021
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6f20efca-943b-4bc2-a157-0931bd4d4585