NDC 71335-1235 – Losartan Potassium

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

Human Prescription Drug

Product NDC71335-1235

Product details

Brand name
Losartan Potassium
Generic name
Losartan Potassium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090083
Marketed since
October 6, 2010
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
71335-1235-130 TABLET, FILM COATED in 1 BOTTLE (71335-1235-1)May 30, 2019
71335-1235-260 TABLET, FILM COATED in 1 BOTTLE (71335-1235-2)Jul 9, 2024
71335-1235-390 TABLET, FILM COATED in 1 BOTTLE (71335-1235-3)Jun 21, 2019
71335-1235-4120 TABLET, FILM COATED in 1 BOTTLE (71335-1235-4)Jul 9, 2024
71335-1235-5100 TABLET, FILM COATED in 1 BOTTLE (71335-1235-5)Jul 9, 2024
71335-1235-628 TABLET, FILM COATED in 1 BOTTLE (71335-1235-6)Jul 9, 2024
71335-1235-710 TABLET, FILM COATED in 1 BOTTLE (71335-1235-7)Sep 3, 2019
71335-1235-8180 TABLET, FILM COATED in 1 BOTTLE (71335-1235-8)Jul 9, 2024

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