NDC 42708-193 – Losartan Potassium and Hydrochlorothiazide

Losartan Potassium 50 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC42708-193

Product details

Brand name
Losartan Potassium and Hydrochlorothiazide
Generic name
Losartan potassium and hydrochlorothiazide
Labeler
QPharma, Inc
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204901
Marketed since
February 15, 2018
Listing expires
December 31, 2027
Pharmacologic class
Angiotensin 2 Receptor Blocker; Thiazide Diuretic

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
42708-193-30 sample30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-193-30)Feb 1, 2026

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