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
68071-4435_1a8c4db5-140d-1e19-e063-6294a90ae99c
Product NDC
68071-4435
Form
TABLET
Composition / generic term
Lisinopril and Hydrochlorothiazide
Labeler
NuCare Pharmaceuticals,Inc.
Marketing category
ANDA
Marketing start / end (source format)
20030304
Source listing expiry
20261231

Source-listed ingredients

  • LISINOPRIL — 20 mg/1
  • HYDROCHLOROTHIAZIDE — 12.5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE (68071-4435-3) · 68071-4435-3
  • 60 TABLET in 1 BOTTLE (68071-4435-6) · 68071-4435-6
  • 90 TABLET in 1 BOTTLE (68071-4435-9) · 68071-4435-9

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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