NDC 68180-215 – Losartan Potassium and Hydrochlorothiazide

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

Human Prescription Drug 3 recalls

Product NDC68180-215

Product details

Brand name
Losartan Potassium and Hydrochlorothiazide
Generic name
Losartan Potassium and Hydrochlorothiazide
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078245
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 (2)

Package NDCDescriptionSince
68180-215-0630 TABLET in 1 BOTTLE (68180-215-06)Oct 6, 2010
68180-215-0990 TABLET in 1 BOTTLE (68180-215-09)Oct 6, 2010

Recalls mentioning this NDC

Other Losartan Potassium and Hydrochlorothiazide products