# Amlodipine and Benazepril Hydrochloride

NDC: 84677-013
Generic name: Amlodipine and Benazepril Hydrochloride
Labeler / Manufacturer: Golden State Medical Supply, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20131230

FDA application: ANDA091431

## Active ingredients

- AMLODIPINE BESYLATE: 10 mg/1
- BENAZEPRIL HYDROCHLORIDE: 40 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"84677-013"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=84677-013
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=47acdbff-b538-9edc-e063-6394a90a3e3b