# Amlodipine Besylate and Benazepril Hydrochloride

NDC: 50090-5137
Generic name: Amlodipine Besylate and Benazepril Hydrochloride
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20100419

FDA application: ANDA077183

## 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:"50090-5137"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-5137
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7a75935a-31af-4571-b7d9-8c297a635b57