# Enalapril Maleate and Hydrochlorothiazide

NDC: 51672-4045
Generic name: Enalapril Maleate and Hydrochlorothiazide
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: 20010918

FDA application: ANDA075788

## Active ingredients

- ENALAPRIL MALEATE: 5 mg/1
- HYDROCHLOROTHIAZIDE: 12.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-4045"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-4045
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7cb92cf2-46f2-4379-937c-168d230e43a4