# ENALAPRIL MALEATE

NDC: 50090-7677
Generic name: ENALAPRIL MALEATE
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250212

FDA application: ANDA075178

## Active ingredients

- ENALAPRIL MALEATE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-7677"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-7677
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fd0a7ecc-d6a2-4e04-a14f-1ed4dacb7df3