NDC 68788-4127 – Losartan potassium

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

Human Prescription Drug

Product NDC68788-4127

Product details

Brand name
Losartan potassium
Generic name
Losartan potassium
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202230
Marketed since
June 9, 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 (2)

Package NDCDescriptionSince
68788-4127-330 TABLET, FILM COATED in 1 BOTTLE (68788-4127-3)Jun 9, 2026
68788-4127-990 TABLET, FILM COATED in 1 BOTTLE (68788-4127-9)Jun 9, 2026

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