# Amlodipine Besylate and Benazepril Hydrochloride

NDC: 51655-201
Generic name: Amlodipine Besylate and Benazepril Hydrochloride
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20230419

FDA application: ANDA077183

## Active ingredients

- AMLODIPINE BESYLATE: 5 mg/1
- BENAZEPRIL HYDROCHLORIDE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-201"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-201
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fa153720-b24c-60d0-e053-6294a90a97d5