NDC 71335-1644 – Losortan Potassium

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

Human Prescription Drug

Product NDC71335-1644

Product details

Brand name
Losortan Potassium
Generic name
Losartan Potassium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078243
Marketed since
October 4, 2010
Listing expires
December 31, 2027
Pharmacologic class
Angiotensin 2 Receptor Blocker

Active ingredients

Uses, dosage, side effects and warnings for Losortan Potassium →

Package NDC codes (6)

Package NDCDescriptionSince
71335-1644-190 TABLET, FILM COATED in 1 BOTTLE (71335-1644-1)Jul 9, 2020
71335-1644-230 TABLET, FILM COATED in 1 BOTTLE (71335-1644-2)Jul 1, 2020
71335-1644-360 TABLET, FILM COATED in 1 BOTTLE (71335-1644-3)Sep 9, 2020
71335-1644-4100 TABLET, FILM COATED in 1 BOTTLE (71335-1644-4)Feb 14, 2022
71335-1644-510 TABLET, FILM COATED in 1 BOTTLE (71335-1644-5)Feb 14, 2022
71335-1644-67 TABLET, FILM COATED in 1 BOTTLE (71335-1644-6)Feb 14, 2022

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