United States · FDA National Drug Code directory
Lisinopril 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
- 63629-4470_6ae03122-17fd-405e-9951-bac76256e28a
- Product NDC
- 63629-4470
- Form
- TABLET
- Composition / generic term
- Lisinopril and Hydrochlorothiazide
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20061004
- Source listing expiry
- 20271231
Source-listed ingredients
- HYDROCHLOROTHIAZIDE — 12.5 mg/1
- LISINOPRIL — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (63629-4470-1) · 63629-4470-1
- 90 TABLET in 1 BOTTLE (63629-4470-2) · 63629-4470-2
- 100 TABLET in 1 BOTTLE (63629-4470-3) · 63629-4470-3
- 60 TABLET in 1 BOTTLE (63629-4470-4) · 63629-4470-4
- 360 TABLET in 1 BOTTLE (63629-4470-5) · 63629-4470-5
- 4 TABLET in 1 BOTTLE (63629-4470-6) · 63629-4470-6
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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