# Enalapril Maleate

NDC: 72789-318
Generic name: Enalapril Maleate
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220424

FDA application: ANDA213273

## Active ingredients

- ENALAPRIL MALEATE: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72789-318"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72789-318
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cbaaa849-0f9d-4294-b122-090ff17fdcc7