# Enalaprilat

NDC: 0143-9787
Generic name: enalaprilat
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20081223

FDA application: ANDA078687

## Active ingredients

- ENALAPRILAT DIHYDRATE: 1.25 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0143-9787"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-9787
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=eabae489-e254-4987-ab90-7cda20a6f856