# Enalapril maleate

NDC: 51655-058
Generic name: Enalapril maleate
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220711

FDA application: ANDA075479

## Active ingredients

- ENALAPRIL MALEATE: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-058"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-058
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f2a0bd73-0389-3f88-e053-2995a90a72e8