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
43063-812_415b9940-77ea-a174-e063-6294a90a4cfe
Product NDC
43063-812
Form
TABLET
Composition / generic term
Lisinopril
Labeler
PD-Rx Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20170830
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, PLASTIC (43063-812-01) · 43063-812-01
  • 12 TABLET in 1 BOTTLE, PLASTIC (43063-812-12) · 43063-812-12
  • 14 TABLET in 1 BOTTLE, PLASTIC (43063-812-14) · 43063-812-14
  • 30 TABLET in 1 BOTTLE, PLASTIC (43063-812-30) · 43063-812-30
  • 60 TABLET in 1 BOTTLE, PLASTIC (43063-812-60) · 43063-812-60
  • 90 TABLET in 1 BOTTLE, PLASTIC (43063-812-90) · 43063-812-90
  • 180 TABLET in 1 BOTTLE, PLASTIC (43063-812-93) · 43063-812-93
  • 120 TABLET in 1 BOTTLE, PLASTIC (43063-812-98) · 43063-812-98

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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