United States · FDA National Drug Code directory
Lisinopril
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
- 68001-333_c5fac2c4-de1f-49d3-e053-2a95a90a5285
- Product NDC
- 68001-333
- Form
- TABLET
- Composition / generic term
- Lisinopril
- Labeler
- BluePoint Laboratories
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170801
- Source listing expiry
- 20261231
Source-listed ingredients
- LISINOPRIL — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (68001-333-00) · 68001-333-00
- 1000 TABLET in 1 BOTTLE (68001-333-08) · 68001-333-08
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 →