NDC 46708-450 – Losartan Potassium and Hydrochlorothiazide

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

Human Prescription Drug

Product NDC46708-450

Product details

Brand name
Losartan Potassium and Hydrochlorothiazide
Generic name
Losartan Potassium and Hydrochlorothiazide
Labeler
Alembic Pharmaceuticals Limited
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 (4)

Package NDCDescriptionSince
46708-450-10100 BLISTER PACK in 1 CARTON (46708-450-10) / 10 TABLET, FILM COATED in 1 BLISTER PACKMay 23, 2016
46708-450-3030 TABLET, FILM COATED in 1 BOTTLE (46708-450-30)May 23, 2016
46708-450-9090 TABLET, FILM COATED in 1 BOTTLE (46708-450-90)May 23, 2016
46708-450-911000 TABLET, FILM COATED in 1 BOTTLE (46708-450-91)May 23, 2016

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