# Epaned

NDC: 52652-4001
Generic name: enalapril maleate
Labeler / Manufacturer: Azurity Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20161003

FDA application: NDA208686

## Active ingredients

- ENALAPRIL MALEATE: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"52652-4001"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=52652-4001
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e6dbda02-779e-420c-893d-d0fea09432be