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
76282-447_7f4a4f31-58b0-4fe1-bd11-ba5a6ac4f26c
Product NDC
76282-447
Form
TABLET
Composition / generic term
Lisinopril and Hydrochlorothiazide Tablets
Labeler
Exelan Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20190501
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

  • 100 TABLET in 1 BOTTLE (76282-447-01) · 76282-447-01
  • 500 TABLET in 1 BOTTLE (76282-447-05) · 76282-447-05
  • 1000 TABLET in 1 BOTTLE (76282-447-10) · 76282-447-10
  • 90 TABLET in 1 BOTTLE (76282-447-90) · 76282-447-90

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.

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Lisinopril and Hydrochlorothiazide — United States | Molindra Medicines