NDC 63187-394 – Losartan Potassium and Hydrochlorothiazide

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

Human Prescription Drug

Product NDC63187-394

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
63187-394-3030 TABLET, FILM COATED in 1 BOTTLE (63187-394-30)Oct 3, 2016
63187-394-6060 TABLET, FILM COATED in 1 BOTTLE (63187-394-60)Oct 3, 2016
63187-394-9090 TABLET, FILM COATED in 1 BOTTLE (63187-394-90)Oct 3, 2016

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