United States · FDA National Drug Code directory
Quinapril and Hydrochlorothiazide 20/25
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
- 69097-831_4d3f7e7a-ed61-4df6-bc45-f38fb4117406
- Product NDC
- 69097-831
- Form
- TABLET
- Composition / generic term
- Quinapril and Hydrochlorothiazide 20/25
- Labeler
- Cipla USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160720
- Source listing expiry
- 20261231
Source-listed ingredients
- QUINAPRIL HYDROCHLORIDE — 20 mg/1
- HYDROCHLOROTHIAZIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET in 1 BOTTLE (69097-831-05) · 69097-831-05
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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