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
71205-763_84dba61d-cae2-4f21-9a9e-3088f356f838
Product NDC
71205-763
Form
TABLET
Composition / generic term
Lisinopril and Hydrochlorothiazide Tablets
Labeler
Proficient Rx LP
Marketing category
ANDA
Marketing start / end (source format)
20150312
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 (71205-763-30) · 71205-763-30
  • 60 TABLET in 1 BOTTLE (71205-763-60) · 71205-763-60
  • 90 TABLET in 1 BOTTLE (71205-763-90) · 71205-763-90

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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