NDC 71335-0176 – Lisinopril

Lisinopril 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0176

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 (6)

Package NDCDescriptionSince
71335-0176-130 TABLET in 1 BOTTLE (71335-0176-1)Feb 27, 2018
71335-0176-290 TABLET in 1 BOTTLE (71335-0176-2)Mar 16, 2018
71335-0176-360 TABLET in 1 BOTTLE (71335-0176-3)Oct 12, 2022
71335-0176-4100 TABLET in 1 BOTTLE (71335-0176-4)Mar 28, 2018
71335-0176-510 TABLET in 1 BOTTLE (71335-0176-5)Mar 19, 2019
71335-0176-628 TABLET in 1 BOTTLE (71335-0176-6)Oct 8, 2024

Other Lisinopril products