NDC 42708-055 – Losartan Potassium

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

Human Prescription Drug

Product NDC42708-055

Product details

Brand name
Losartan Potassium
Generic name
Losartan Potassium
Labeler
QPharma, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090083
Marketed since
October 6, 2010
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker

Active ingredients

Uses, dosage, side effects and warnings for Losartan potassium →

Package NDC codes (1)

Package NDCDescriptionSince
42708-055-30 sample30 TABLET, FILM COATED in 1 BOTTLE (42708-055-30)Jul 30, 2018

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