# Enalaprilat

NDC: 43598-169
Generic name: enalaprilat
Labeler / Manufacturer: Dr. Reddys Laboratories Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20230606

FDA application: ANDA075578

## Active ingredients

- ENALAPRILAT: 2.5 mg/2mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43598-169"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-169
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5d398da1-020c-ccb1-a775-ce8e0b29d621