# Lisinopril and Hydrochlorothiazide

NDC: 43063-482
Generic name: Lisinopril and Hydrochlorothiazide
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20061004

FDA application: ANDA077912

## Active ingredients

- HYDROCHLOROTHIAZIDE: 12.5 mg/1
- LISINOPRIL: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43063-482"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43063-482
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ec23c75d-68d5-46d0-be56-b96ddba19ed6