NDC 71610-207 – Losartan Potassium

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

Human Prescription Drug

Product NDC71610-207

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 · ANDA091497
Marketed since
July 30, 2014
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 (3)

Package NDCDescriptionSince
71610-207-3030 TABLET, FILM COATED in 1 BOTTLE (71610-207-30)Dec 14, 2018
71610-207-4545 TABLET, FILM COATED in 1 BOTTLE (71610-207-45)Dec 14, 2018
71610-207-6090 TABLET, FILM COATED in 1 BOTTLE (71610-207-60)Dec 14, 2018

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