NDC 71610-083 – Losartan Potassium

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

Human Prescription Drug

Product NDC71610-083

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 · 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 (2)

Package NDCDescriptionSince
71610-083-3030 TABLET, FILM COATED in 1 BOTTLE (71610-083-30)Jun 27, 2018
71610-083-6090 TABLET, FILM COATED in 1 BOTTLE (71610-083-60)Jun 6, 2018

Other Losartan potassium products