# Amlodipine and Benazepril Hydrochloride

NDC: 57237-145
Generic name: Amlodipine and Benazepril Hydrochloride
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20120905

FDA application: ANDA202239

## Active ingredients

- AMLODIPINE BESYLATE: 5 mg/1
- BENAZEPRIL HYDROCHLORIDE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"57237-145"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57237-145
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=03b175fc-d430-490d-b7ac-9f7a2cb1dd8b