# AMLODIPINE AND BENAZEPRIL HYDROCHLORIDE

NDC: 72189-260
Generic name: AMLODIPINE AND BENAZEPRIL HYDROCHLORIDE
Labeler / Manufacturer: DIRECT RX
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20210810

FDA application: ANDA202239

## 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:"72189-260"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72189-260
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b8b9a3cd-c4e7-dfeb-e053-2a95a90aa719