NDC 71335-0536 – Lisinopril

Lisinopril 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0536

Product details

Brand name
Lisinopril
Generic name
Lisinopril
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076164
Marketed since
November 1, 2011
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin Converting Enzyme Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Lisinopril →

Package NDC codes (10)

Package NDCDescriptionSince
71335-0536-010 TABLET in 1 BOTTLE (71335-0536-0)Oct 8, 2024
71335-0536-130 TABLET in 1 BOTTLE (71335-0536-1)Mar 21, 2018
71335-0536-2100 TABLET in 1 BOTTLE (71335-0536-2)Jan 28, 2019
71335-0536-360 TABLET in 1 BOTTLE (71335-0536-3)Aug 20, 2018
71335-0536-490 TABLET in 1 BOTTLE (71335-0536-4)Mar 5, 2018
71335-0536-520 TABLET in 1 BOTTLE (71335-0536-5)Jun 26, 2018
71335-0536-6120 TABLET in 1 BOTTLE (71335-0536-6)Nov 20, 2019
71335-0536-77 TABLET in 1 BOTTLE (71335-0536-7)Mar 21, 2019
71335-0536-815 TABLET in 1 BOTTLE (71335-0536-8)Apr 24, 2018
71335-0536-92 TABLET in 1 BOTTLE (71335-0536-9)Jan 19, 2022

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