NDC 67046-1618 – Losartan Potassium and Hydrochlorothiazide

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

Human Prescription Drug

Product NDC67046-1618

Product details

Brand name
Losartan Potassium and Hydrochlorothiazide
Generic name
Losartan Potassium and Hydrochlorothiazide
Labeler
Coupler LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091629
Marketed since
December 2, 2025
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
67046-1618-330 TABLET, FILM COATED in 1 BLISTER PACK (67046-1618-3)Dec 2, 2025

Other Losartan Potassium and Hydrochlorothiazide products