# Amlodipine Besylate and Benazepril Hydrochloride

NDC: 55111-587
Generic name: Amlodipine Besylate and Benazepril Hydrochloride
Labeler / Manufacturer: Dr.Reddy's Laboratories Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20110705

FDA application: ANDA090149

## 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:"55111-587"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55111-587
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f12f18bb-7ddb-e7dc-4edd-32f4ac212bca