# Enalapril Maleate

NDC: 51672-4037
Generic name: Enalapril Maleate
Labeler / Manufacturer: Taro Pharmaceuticals U.S.A., Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20010123

FDA application: ANDA075657

## Active ingredients

- ENALAPRIL MALEATE: 2.5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-4037"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-4037
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f103b9f9-e081-419d-a2d8-b86acda834dd