# Lisinopril and Hydrochlorothiazide

NDC: 68071-4435
Generic name: Lisinopril and Hydrochlorothiazide
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20030304

FDA application: ANDA076194

## Active ingredients

- HYDROCHLOROTHIAZIDE: 12.5 mg/1
- LISINOPRIL: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-4435"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-4435
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6c57bf12-9ad5-3a25-e053-2a91aa0aaf26