# Amlodipine Besylate

NDC: 72789-514
Generic name: Amlodipine Besylate
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20070523

FDA application: ANDA076719

## Active ingredients

- AMLODIPINE BESYLATE: 2.5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72789-514"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72789-514
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5a0b3dd4-91f5-4173-a992-e91b1cac6a18