NDC 71335-0262 – Losartan Potassium

Losartan Potassium 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-0262

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 (7)

Package NDCDescriptionSince
71335-0262-130 TABLET, FILM COATED in 1 BOTTLE (71335-0262-1)Apr 22, 2019
71335-0262-290 TABLET, FILM COATED in 1 BOTTLE (71335-0262-2)Apr 3, 2019
71335-0262-360 TABLET, FILM COATED in 1 BOTTLE (71335-0262-3)Jan 20, 2022
71335-0262-4120 TABLET, FILM COATED in 1 BOTTLE (71335-0262-4)Jan 20, 2022
71335-0262-5100 TABLET, FILM COATED in 1 BOTTLE (71335-0262-5)Jan 20, 2022
71335-0262-6180 TABLET, FILM COATED in 1 BOTTLE (71335-0262-6)Jan 20, 2022
71335-0262-710 TABLET, FILM COATED in 1 BOTTLE (71335-0262-7)Jan 20, 2022

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