NDC 50090-5960 – Losartan Potassium and Hydrochlorothiazide

Losartan Potassium 100 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC50090-5960

Product details

Brand name
Losartan Potassium and Hydrochlorothiazide
Generic name
Losartan potassium and hydrochlorothiazide
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA201845
Marketed since
October 30, 2012
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker; Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Losartan Potassium and Hydrochlorothiazide →

Package NDC codes (3)

Package NDCDescriptionSince
50090-5960-030 TABLET, FILM COATED in 1 BOTTLE (50090-5960-0)Apr 11, 2022
50090-5960-190 TABLET, FILM COATED in 1 BOTTLE (50090-5960-1)Apr 11, 2022
50090-5960-2100 TABLET, FILM COATED in 1 BOTTLE (50090-5960-2)Mar 9, 2023

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