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
- 72865-210_c008ecb6-970d-4ac9-9402-e21e8d9d76b2
- Product NDC
- 72865-210
- Form
- TABLET
- Composition / generic term
- Lisinopril
- Labeler
- XLCare Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210817
- Source listing expiry
- 20261231
Source-listed ingredients
- LISINOPRIL — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (72865-210-01) · 72865-210-01
- 1000 TABLET in 1 BOTTLE (72865-210-10) · 72865-210-10
- 45 TABLET in 1 BOTTLE (72865-210-45) · 72865-210-45
- 5000 TABLET in 1 BOTTLE (72865-210-50) · 72865-210-50
- 90 TABLET in 1 BOTTLE (72865-210-90) · 72865-210-90
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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