United States · FDA National Drug Code directory
benazepril hydrochloride and hydrochlorothiazide
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0574-0228_55072852-c532-448e-935e-102e981cf698
- Product NDC
- 0574-0228
- Form
- TABLET
- Composition / generic term
- benazepril hydrochloride and hydrochlorothiazide
- Labeler
- Padagis US LLC
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20190407 / 20270331
Source-listed ingredients
- BENAZEPRIL HYDROCHLORIDE — 20 mg/1
- HYDROCHLOROTHIAZIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (0574-0228-01) · 0574-0228-01
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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