NDC 71335-1102 – Losartan Potassium

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

Human Prescription Drug

Product NDC71335-1102

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 (8)

Package NDCDescriptionSince
71335-1102-130 TABLET, FILM COATED in 1 BOTTLE (71335-1102-1)Mar 16, 2016
71335-1102-290 TABLET, FILM COATED in 1 BOTTLE (71335-1102-2)Mar 16, 2016
71335-1102-360 TABLET, FILM COATED in 1 BOTTLE (71335-1102-3)Mar 16, 2016
71335-1102-4120 TABLET, FILM COATED in 1 BOTTLE (71335-1102-4)Mar 16, 2016
71335-1102-5100 TABLET, FILM COATED in 1 BOTTLE (71335-1102-5)Mar 16, 2016
71335-1102-6180 TABLET, FILM COATED in 1 BOTTLE (71335-1102-6)Mar 16, 2016
71335-1102-710 TABLET, FILM COATED in 1 BOTTLE (71335-1102-7)Mar 16, 2016
71335-1102-87 TABLET, FILM COATED in 1 BOTTLE (71335-1102-8)Mar 16, 2016

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