NDC 71335-1582 – Losartan Potassium

Losartan Potassium 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-1582

Product details

Brand name
Losartan Potassium
Generic name
Losartan Potassium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203835
Marketed since
August 19, 2015
Listing expires
December 31, 2027
Pharmacologic class
Angiotensin 2 Receptor Blocker

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
71335-1582-190 TABLET, FILM COATED in 1 BOTTLE (71335-1582-1)Apr 30, 2020
71335-1582-230 TABLET, FILM COATED in 1 BOTTLE (71335-1582-2)Apr 30, 2020
71335-1582-360 TABLET, FILM COATED in 1 BOTTLE (71335-1582-3)Apr 30, 2020
71335-1582-4100 TABLET, FILM COATED in 1 BOTTLE (71335-1582-4)Apr 30, 2020
71335-1582-510 TABLET, FILM COATED in 1 BOTTLE (71335-1582-5)Apr 30, 2020
71335-1582-67 TABLET, FILM COATED in 1 BOTTLE (71335-1582-6)Apr 30, 2020

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