NDC 68788-4007 – Losartan Potassium

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

Human Prescription Drug

Product NDC68788-4007

Product details

Brand name
Losartan Potassium
Generic name
Losartan Potassium
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091497
Marketed since
August 8, 2025
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 (5)

Package NDCDescriptionSince
68788-4007-1100 TABLET, FILM COATED in 1 BOTTLE (68788-4007-1)Aug 8, 2025
68788-4007-330 TABLET, FILM COATED in 1 BOTTLE (68788-4007-3)Aug 8, 2025
68788-4007-550 TABLET, FILM COATED in 1 BOTTLE (68788-4007-5)Aug 8, 2025
68788-4007-660 TABLET, FILM COATED in 1 BOTTLE (68788-4007-6)Aug 8, 2025
68788-4007-990 TABLET, FILM COATED in 1 BOTTLE (68788-4007-9)Aug 8, 2025

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