NDC 71335-2083 – Losartan Potassium

Losartan Potassium 100 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-2083

Product details

Brand name
Losartan Potassium
Generic name
Losartan Potassium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091497
Marketed since
July 30, 2014
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker

Active ingredients

Uses, dosage, side effects and warnings for Losartan potassium →

Package NDC codes (8)

Package NDCDescriptionSince
71335-2083-130 TABLET, FILM COATED in 1 BOTTLE (71335-2083-1)Apr 14, 2023
71335-2083-260 TABLET, FILM COATED in 1 BOTTLE (71335-2083-2)Apr 14, 2023
71335-2083-390 TABLET, FILM COATED in 1 BOTTLE (71335-2083-3)Apr 14, 2023
71335-2083-4120 TABLET, FILM COATED in 1 BOTTLE (71335-2083-4)Apr 14, 2023
71335-2083-5100 TABLET, FILM COATED in 1 BOTTLE (71335-2083-5)Apr 14, 2023
71335-2083-628 TABLET, FILM COATED in 1 BOTTLE (71335-2083-6)Apr 14, 2023
71335-2083-710 TABLET, FILM COATED in 1 BOTTLE (71335-2083-7)Apr 14, 2023
71335-2083-8180 TABLET, FILM COATED in 1 BOTTLE (71335-2083-8)Apr 14, 2023

Other Losartan potassium products