NDC 72189-012 – Losartan Potassium And Hydrochlorothiazide

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

Human Prescription Drug 1 recall

Product NDC72189-012

Product details

Brand name
Losartan Potassium And Hydrochlorothiazide
Generic name
Losartan Potassium And Hydrochlorothiazide
Labeler
Direct_Rx
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091629
Marketed since
July 17, 2019
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 (1)

Package NDCDescriptionSince
72189-012-9090 TABLET, FILM COATED in 1 BOTTLE (72189-012-90)Jul 17, 2019

Recalls mentioning this NDC

Other Losartan Potassium and Hydrochlorothiazide products