NDC 50090-1641 – Losartan Potassium and Hydrochlorothiazide

Losartan Potassium 100 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC50090-1641

Product details

Brand name
Losartan Potassium and Hydrochlorothiazide
Generic name
Losartan Potassium and Hydrochlorothiazide
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091629
Marketed since
October 6, 2010
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
50090-1641-030 TABLET, FILM COATED in 1 BOTTLE (50090-1641-0)Jan 15, 2015
50090-1641-190 TABLET, FILM COATED in 1 BOTTLE (50090-1641-1)Jan 15, 2015
50090-1641-2100 TABLET, FILM COATED in 1 BOTTLE (50090-1641-2)Aug 2, 2024

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