# Amlodipine Besylate

NDC: 43063-041
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: 20101020

FDA application: ANDA078925

## Active ingredients

- AMLODIPINE BESYLATE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43063-041"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43063-041
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=47114f60-4151-43d4-ac2d-adc49492a679
