NDC 87441-053 – Losartan Potassium

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

Human Prescription Drug

Product NDC87441-053

Product details

Brand name
Losartan Potassium
Generic name
Losartan Potassium
Labeler
Unit Dose Solutions, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090083
Marketed since
June 26, 2026
Listing expires
December 31, 2027
Pharmacologic class
Angiotensin 2 Receptor Blocker

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
87441-053-0130 TABLET, FILM COATED in 1 BLISTER PACK (87441-053-01)Jun 26, 2026

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