NDC 63187-918 – Losartan Potassium and Hydrochlorothiazide

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

Human Prescription Drug

Product NDC63187-918

Product details

Brand name
Losartan Potassium and Hydrochlorothiazide
Generic name
Losartan Potassium and Hydrochlorothiazide
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091617
Marketed since
May 23, 2016
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 (3)

Package NDCDescriptionSince
63187-918-3030 TABLET, FILM COATED in 1 BOTTLE (63187-918-30)Oct 2, 2017
63187-918-6060 TABLET, FILM COATED in 1 BOTTLE (63187-918-60)Oct 2, 2017
63187-918-9090 TABLET, FILM COATED in 1 BOTTLE (63187-918-90)Oct 2, 2017

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