NDC 31722-755 – Losartan Potassium And Hydrochlorothiazide

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

Human Prescription Drug

Product NDC31722-755

Product details

Brand name
Losartan Potassium And Hydrochlorothiazide
Generic name
Losartan Potassium And Hydrochlorothiazide
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA219869
Marketed since
May 27, 2026
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 (3)

Package NDCDescriptionSince
31722-755-101000 TABLET, FILM COATED in 1 BOTTLE (31722-755-10)May 27, 2026
31722-755-3030 TABLET, FILM COATED in 1 BOTTLE (31722-755-30)May 27, 2026
31722-755-9090 TABLET, FILM COATED in 1 BOTTLE (31722-755-90)May 27, 2026

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