NDC 71610-439 – Losartan Potassium

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

Human Prescription Drug

Product NDC71610-439

Product details

Brand name
Losartan Potassium
Generic name
Losartan Potassium
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203835
Marketed since
March 13, 2020
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 (4)

Package NDCDescriptionSince
71610-439-1515 TABLET, FILM COATED in 1 BOTTLE (71610-439-15)Apr 27, 2021
71610-439-3030 TABLET, FILM COATED in 1 BOTTLE (71610-439-30)Jun 24, 2020
71610-439-4545 TABLET, FILM COATED in 1 BOTTLE (71610-439-45)Mar 15, 2021
71610-439-6090 TABLET, FILM COATED in 1 BOTTLE (71610-439-60)Oct 17, 2022

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