NDC 72189-327 – Losartan Potassium And Hydrochlorothiazide

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

Human Prescription Drug

Product NDC72189-327

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 · ANDA204901
Marketed since
February 17, 2022
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 (2)

Package NDCDescriptionSince
72189-327-3030 TABLET, FILM COATED in 1 BOTTLE (72189-327-30)Feb 17, 2022
72189-327-9090 TABLET, FILM COATED in 1 BOTTLE (72189-327-90)Feb 17, 2022

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