NDC 50090-2622 – Losartan Potassium

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

Human Prescription Drug

Product NDC50090-2622

Product details

Brand name
Losartan Potassium
Generic name
Losartan Potassium
Labeler
A-S Medication Solutions
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 (3)

Package NDCDescriptionSince
50090-2622-030 TABLET, FILM COATED in 1 BOTTLE (50090-2622-0)Dec 7, 2016
50090-2622-190 TABLET, FILM COATED in 1 BOTTLE (50090-2622-1)Nov 16, 2016
50090-2622-2100 TABLET, FILM COATED in 1 BOTTLE (50090-2622-2)Oct 26, 2023

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