# Amlodipine Besylate and Benazepril Hydrochloride

NDC: 68180-472
Generic name: Amlodipine Besylate and Benazepril Hydrochloride
Labeler / Manufacturer: Lupin Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20180801

FDA application: ANDA078466

## Active ingredients

- AMLODIPINE BESYLATE: 10 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:"68180-472"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68180-472
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=968c611b-43a7-40f0-9ed3-aa67ee88364b