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
- 68462-579_51b0aed8-a229-4d2c-8fdf-aa957fddc41b
- Product NDC
- 68462-579
- Form
- TABLET, FILM COATED
- Composition / generic term
- Benazepril Hydrochloride and Hydrochlorothiazide
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20040211
- Source listing expiry
- 20261231
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, FILM COATED in 1 BOTTLE (68462-579-01) · 68462-579-01
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →